0001185185-17-000445.txt : 20170224 0001185185-17-000445.hdr.sgml : 20170224 20170224160704 ACCESSION NUMBER: 0001185185-17-000445 CONFORMED SUBMISSION TYPE: 8-K PUBLIC DOCUMENT COUNT: 5 CONFORMED PERIOD OF REPORT: 20170221 ITEM INFORMATION: Entry into a Material Definitive Agreement ITEM INFORMATION: Financial Statements and Exhibits FILED AS OF DATE: 20170224 DATE AS OF CHANGE: 20170224 FILER: COMPANY DATA: COMPANY CONFORMED NAME: Entia Biosciences, Inc. CENTRAL INDEX KEY: 0001408299 STANDARD INDUSTRIAL CLASSIFICATION: MEDICINAL CHEMICALS & BOTANICAL PRODUCTS [2833] IRS NUMBER: 260561199 STATE OF INCORPORATION: NV FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 8-K SEC ACT: 1934 Act SEC FILE NUMBER: 000-52864 FILM NUMBER: 17637198 BUSINESS ADDRESS: STREET 1: 13565 SW TUALATIN-SHERWOOD RD. STREET 2: SUITE 800 CITY: SHERWOOD STATE: OR ZIP: 97140 BUSINESS PHONE: 971-228-0709 MAIL ADDRESS: STREET 1: 13565 SW TUALATIN-SHERWOOD RD. STREET 2: SUITE 800 CITY: SHERWOOD STATE: OR ZIP: 97140 FORMER COMPANY: FORMER CONFORMED NAME: Total Nutraceutical Solutions, Inc. DATE OF NAME CHANGE: 20090608 FORMER COMPANY: FORMER CONFORMED NAME: Total Nutraceutical Solutions DATE OF NAME CHANGE: 20081024 FORMER COMPANY: FORMER CONFORMED NAME: Generic Marketing Services, Inc. DATE OF NAME CHANGE: 20070730 8-K 1 entiabiosciences8k022416.htm 8-K

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549
 

 
FORM 8-K
 

 
CURRENT REPORT
 
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
 
Date of Report (Date of Earliest Event Reported): February 21, 2017
 
Entia Biosciences, Inc.
 (Exact name of registrant as specified in charter)
 
Commission File Number:   000-52864
 
Nevada
26-0561199
(State or other jurisdiction of
incorporation or organization)
(I.R.S. Employer Identification No.)

13565 SW Tualatin-Sherwood Road, Suite 800
Sherwood, Oregon
97140
(Address of principal executive offices)
(Zip Code)

(971) 228-0709
(Registrant’s telephone number, including area code)
 
                                                                                                               
(Former name or former address, if changed since last report)
 
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
 
   Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
 
   Soliciting material pursuant to Rule 14a-12 under the Exchange Act(17CFR240.14a-12)
 
   Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act(17CFR240.14d-2(b))
 
   Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act(17CFR240.13e-4(c))


Item 1.01 Entry into a Material Definitive Agreement
On February 21, 2017, we received an executed, definitive licensing agreement (the “License”) with GROH Beauty Corp (the “Licensee”) under which we granted certain exclusive worldwide rights to manufacture and distribute our GROH beauty products.  The License calls for a front-end license fee, half of which is non-refundable and the other half of which is subject to a number of factors during a due diligence period, as well as royalties over a period of years, also subject to the completion of the due diligence period, until the license is paid in full and thereby becomes an exclusive perpetual license of the Licensee.  The total value of the license fees and royalties to us is $1,150,000.  The License calls for and was accompanied by a separate executed agreement under which we are to manufacture and sell our ErgoD2® compound exclusively to the Licensee for its use in the cosmetic and beauty care markets.  As this manufacturing agreement provides for price adjustments and is expected to run for a number of future years concurrent with the License, its positive value to us is inestimable at this time.  Additionally, the License calls for a separate agreement through which our Chief Science and Technology Officer, Dr. Marvin Hausman, will provide consulting services to the Licensee.

Item 9.01 Financial Statements and Exhibits
 

Exhibit No.
Description
99.1
99.2
99.3
 
†             Confidential treatment has been requested for portions of these exhibits. These portions have been omitted and filed separately with the Securities and Exchange Commission.



 
SIGNATURES

 
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
 
 
ENTIA BIOSCIENCES, INC.
 
 
(Registrant)
 
 
 
 
 
Date: February 24, 2017
By:
/s/ Carl Johnson
 
 
 
Carl Johnson
 
 
 
President and CEO
 
 
 
 
 
 
 


†             Confidential treatment has been requested for portions of these exhibits. These portions have been omitted and filed separately with the Securities and Exchange Commission.


EX-99.1 2 ex99-1.htm EX-99.1
 
EXHIBIT 99.1



Press Release – for release February 24, 2017


Entia Biosciences, Inc. (OTCQB: ERGO) Enters into Exclusive Worldwide Licensing Agreement for its GROH Beauty Products Line

PORTLAND, Oregon -- (GlobeNewswire) –Entia Biosciences, Inc. (OTCQB: ERGO) announced that it has licensed to GROH BEAUTY CORP of Deerfield Beach, Florida, the exclusive worldwide rights to manufacture and distribute its proprietary GROH® beauty care product line.  The license also has a companion agreement that provides for Entia to manufacture and supply its proprietary ErgoD2® product for use in GROH BEAUTY CORP’s manufacture of the various products within the GROH product line.  Together, the license and its companion manufacturing agreement provide Entia with an upfront license fee, on-going royalties based on sales of products containing the ErgoD2 compound and sales revenue from supply of ErgoD2 to GROH BEAUTY CORP.

“We are very pleased to be working with GROH BEAUTY CORP, a new business unit of a proven, successful developer and marketer of beauty and cosmetic products,” stated Carl J. Johnson, President and Chief Executive of Entia.  “We are confident that they will generate significant success with the GROH brand and look forward to the additional resources that this license will provide to us.  This is an alternative but superior approach for Entia to the beauty care market and will better contribute to building value for our shareholders than the Company’s previous efforts in this area.”

Enita’s 2014 entry into the beauty care market did not achieve the success for which the then management had hoped.  Entia’s new management has determined that beauty care is not an appropriate area of strategic focus for the Company, planning instead upon developing and profitably marketing clinically-proven health care products that are based upon the Company’s novel and proprietary ErgoD2 technology in the nutritional supplement and/or medical food categories.

The Company is taking aggressive yet carefully planned steps toward that end.  Dr. Marvin Hausman, Chief Science & Technology Officer, indicated that Entia plans to introduce its first healthcare product before mid-2017.  The product will likely be introduced as a kidney health supplement.  Kidney health is a growing concern in the U.S. and around the world.  “The Company’s research studies among individuals with compromised kidney function have been quite encouraging, if not downright exciting,” noted Hausman.  “We are anxiously looking forward to the market rollout of the first of our new healthcare products.”

“We are delighted to be working with Entia Biosciences and taking over the GROH brand,” said Mr. Patrick Neville of GROH BEAUTY CORP.  “With Entia’s proprietary ErgoD2 compound, the products have characteristics that the beauty market will find quite desirable.  We plan on making GROH a big winner.”

GROH BEAUTY CORP plans on its initial GROH rollout by midyear.  In the interim, GROH products will still be available from Entia through existing channels.


About Entia Biosciences, Inc.

Entia (OTCQB: ERGO) discovers, scientifically validates, develops and markets patented, pharmaceutical-grade organic compounds that include its revolutionary ErgoD2®.  The Company is a leading authority on the clinical effects of oxidative stress, iron-related disorders and free radical reactions in mammals; it is bringing this expertise to the nutraceutical and medical foods markets.  Entia also develops and markets health-related cosmeceuticals.
Entia Biosciences, Inc. is headquartered in Sherwood, Oregon, a Portland suburb.

About GROH BEAUTY CORP

GROH BEAUTY CORP is a newly established business unit of an international developer, manufacturer and marketer of fine beauty products.  It is based in Deerfield Beach, Florida.

Forward-Looking Statements

Any statements contained in this press release that relate to future plans, events or performance are forward-looking statements that involve risks and uncertainties including, but not limited to, the risks associated with the transaction described in this press release, and other risks identified in the filings by Entia Biosciences, Inc. with the Securities and Exchange Commission.  Further information on risks faced by the Company and its shareholders are detailed in the Form 10-K for the year ended December 31, 2015 and in its subsequent Quarterly Reports on Form 10-Q.  These filings are or will become available on a website maintained by the Securities and Exchange Commission at http://www.sec.gov.  The information contained in this press release is accurate as of the date indicated.  Actual results, events or performance may differ materially.  Entia does not undertake any obligation to publicly release the result of any revision to these forward-looking statements that may be made to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.

Contact:

Entia Biosciences, Inc.:   Carl Johnson or Tim Timmins (844-559-9910)

EX-99.2 3 ex99-2.htm EX-99.2
 
EXHIBIT 99.2
 
Pursuant to 17 CFR 240.24b-2, confidential information has been omitted in the places marked ‘[***]’ and has been filed separately with the Securities and Exchange Commission pursuant to a Confidential Treatment Application filed with the Commission.

LICENSE AGREEMENT

This LICENSE AGREEMENT (the “Agreement”) is dated as of the date of the last signature below (the “Effective Date”), by and between Entia Biosciences, Inc. of 13565 SW Tualatin-Sherwood Rd. Suite 800, Sherwood, Oregon 97140 (“Licensor”) and GROH BEAUTY CORP of 508 SW 12th Avenue, Deerfield Beach, Florida 33442 (“Licensee”).  Licensor and/or Licensee are sometimes individually referred to as a “Party” and collectively as the “Parties”.
 
WHEREAS, Licensor owns and/or is the exclusive licensee of the rights in the Compound and regularly produces the Compound for sale to third parties and Licensor wishes to sell the Compound to Licensee;

WHEREAS, Licensee wishes to purchase the Compound from Licensee for use in producing the Articles;

WHEREAS, Licensor has developed Formulations using the Compound to produce the Existing Products for the treatment of hair, skin and anti-aging, and owns certain Trademarks, and Licensor wishes to license to Licensee the Formulations, Trademarks and certain other rights; and

WHEREAS, Licensee wishes to license from Licensor the Formulations, Trademarks and certain other rights.

NOW, THEREFORE, for good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, the Parties agree as follows:

1. Definitions:

(a) “Articles” means cosmetics, beauty care, and supplements and nutraceutical products that are within the Fields of Use and made with the Compound.

(b) “Compound” means that compound derived from mushrooms covered by the Patents and produced by the Method of Production in either powder form currently known as ErgoD2 powder or liquid form currently known as ErgoD2 water.

(c) “Confidential Information” means any and all proprietary information belonging to the disclosing party, whether tangible or intangible, written or oral, including, without limitation, books and records, computer software and files, lists of (or proprietary information concerning) its customers, suppliers, vendors and other business relationships, and any other item which may properly be classified as a protected trade secret.

(d) “Copyrights” means those works set forth or described on Schedule A of this Agreement, which schedule is incorporated by this reference and which may be amended from time to time by the mutual written agreement of the Parties.

(e) “Existing Products” means those Articles set forth on Schedule B, which schedule is incorporated by this reference and which may be amended from time to time by the mutual written agreement of the Parties.


(f) “Fields of Use” means the cosmetics and beauty care markets, the supplement and nutraceutical markets, to the extent these are related to cosmetics and beauty care and including, without limitation, hair care, skin care and anti-aging.

(g) “Formulations” means those formulae and processes developed by Licensor for use of the Compound in the production of the Existing Products, including modifications made to such formulae and processes for any reason, including, but not limited, to addressing the scarcity of any component in the formulation or any governmental restriction that prohibits the sale of the unmodified formulation for any reason.  Formulations expressly exclude formulae and processes used by Licensor in manufacturing the Compound itself.

(h) “Method of Production” means Licensor’s proprietary method of producing the Compound through its proprietary procedures, trade secrets and patented technologies.

(i) “Net Sales” means the total revenues based on gross invoiced sales of Articles, excluding sales and similar taxes, discounts, allowances, credits for returns, rebates, import duties and other governmental charges, freight and transportation charges, and insurance.  For cases in which Articles are sold by Licensee in combination (packaged inseparably) with other Licensee products, Net Sales, for purposes of determining royalty payments on such combination, shall be calculated based on the reasonable portion of the Net Sales price attributable to the Articles.

(j) “Patents” means those patents set forth on Schedule C of this Agreement, which schedule is incorporated by this reference and which may be amended from time to time by the mutual written agreement of the Parties, together with all continuations or continuations-in-part, divisionals, reissues and re-examinations and any rights in any other patents resulting from or claiming a priority from the patents listed in Schedule C.

(k) “Technology” means the Patents and the Method of Production.

(l) “Term” means the time period beginning on the Effective Date and ending on the date that is expiration date of the last Patent.

(m) “Territory” means the world.

(n) “Trademarks” means the trade names, trademarks, service marks, and other indicia set forth on Schedule D of this Agreement, which schedule is incorporated by this reference and which may be amended from time to time by the mutual written agreement of the Parties.

2. Grant of Rights:

(a) During the Term and within the Territory, Licensor hereby grants to Licensee, and Licensee hereby accepts from Licensor, the exclusive, sublicenseable, assignable and non-revocable right and license, but, except as noted in 2(a)(i) below, not the obligation, to:

(i) use the Compound in the Fields of Use including, without limitation, in the production of the Existing Products, provided such use results in Net Sales prior to a date 180 days from the Effective Date;


(ii) make and have made, to use and have used, to sell and have sold, to offer to sell, in the Fields of Use and the right to practice or have practiced the Formulations, as well as methods for making and using the Formulations in the Fields of Use;

(iii) with respect to the Articles and other Licensee products, solely within the Fields of Use, employ the Trademarks: (a) in connection with the manufacture, promotion, sale and distribution thereof; (b) on all packaging materials, containers and promotional materials related thereto; and (c) in connection with the publicity, sales and advertising of thereof, including online, in newspapers, magazines, radio, television, cinema and similar media presently existing or that may exist in the future, subject to:

(A) reasonable requirements by the Licensor as to quality, manufacturing, packaging and notice standards for such Articles; and

(B)  when used alone (away from the word “GROH”), “ErgoD2” will be accompanied by words such as “includes” or “powered by,” along with an acknowledgement the ErgoD2 is a registered trademark of Entia Biosciences, Inc. or its successors and assigns.

(iv) reproduce, prepare derivative works of, distribute copies of, perform publicly and display publicly the Copyrights.

(b) Without limiting the generality of the foregoing, and for the avoidance of doubt, Licensor shall not, during the Term, grant any rights to any third party in connection with the Articles or other products within the Fields of Use, for the Trademark, provided that Licensor retains the right to use “Created by nature, Unlocked by science” in all other fields, including, but not necessarily limited to allopathic and homeopathic pharmaceuticals, medical foods, supplements and nutraceuticals.

3. Licensor’s Additional Covenants:

During the Term, Licensor shall:

 (a) not sell the Compound in powder or liquid form to any third party intended for use in the Fields of Use;

(b) not compete with Licensee in any commercial or business venture regarding the development and marketing of the Formulations in the Fields of Use.

(c) use its best efforts to ascertain whether buyers of its Compound will use the Compound in the Fields of Use; and

(d) immediately discontinue selling the Compound to any buyers that are discovered to be using the Compound in the Fields of Use.

4. License Fee:

In exchange for the rights granted by the Licensor to the Licensee in this Agreement, Licensee shall pay to Licensor the following:

(a) Initial license fee of [***] (the “Initial License Fee”), to be payable on the following schedule:

(i) [***] promptly on the Effective Date of this Agreement; and


(ii) [***] no later than five business days following the earlier of either: (A) Licensee’s first commercial shipment of Articles; or (B) April 1, 2017 (the “First Shipment Date”), provided that such payment is expressly subject to the provisions of Section 11 hereof.

(b) The following royalties (collectively, the “Royalties”):

(i) During the year beginning on the First Shipment Date and ending one (1) twelve month period thereafter: the greater of either: (A) [***]; or (B) [***] percent ([***]%) of Net Sales of  (the “Year One Minimum”).

(ii) During the year beginning on the date that is one (1) year after the First Shipment Date and ending one (1) twelve-month period thereafter: the greater of either: (A) [***]; or (B) [***] percent ([***]%) of Net Sales (the “Year Two Minimum”).

(iii) During the year beginning on the date that is two (2) years after the First Shipment Date and ending one (1) twelve-month period thereafter: the greater of either: (A) [***]; or (B) [***] percent ([***]%) of Net Sales (the “Year Three Minimum”).

(iv) During the year beginning on the date that is three (3) years after the First Shipment Date and ending one (1) twelve month period thereafter: the greater of either: (A) [***]; or (B) [***] percent ([***]%) of Net Sales (the “Year Four Minimum”).

(v) During the year beginning on the date that is four (4) years after the First Shipment Date and ending one (1) twelve-month period thereafter: the greater of either: (A) [***]; or (B) [***] percent ([***]%) of Net Sales (the “Year Five Minimum”).

(vi) During the year beginning on the date that is five (5) years after the First Shipment Date and ending one (1) twelve-month period thereafter: the greater of either: (A) [***]; or (B) [***] percent ([***]%) of Net Sales (the “Year Six Minimum”).

(c) For the avoidance of doubt, in the event that [***] percent ([***]%) of Net Sales exceed [***] in a twelve month period, the excess thereof will be applied to the next twelve-month period’s minimum Royalties.

(d) In the event that Licensee fails to meet the foregoing yearly minimums, Licensor’s sole remedy is to terminate this Agreement according to Section 14(b).

(e) Notwithstanding anything to the contrary contained elsewhere in this Agreement, in the event that the Royalties exceed [***], which amount is exclusive of the Initial License Fee, Licensee shall have paid up license and there will be no further royalty requirements.

5. Contract for Sales of the Compound:

The parties agree to negotiate in good faith for a contract for sales of the Compound by Licensor to Licensee having the following material terms:

(a) Licensor shall provide a discounted sales price for the Compound as follows: (i) the dry powder form of ErgoD2 at an initial cost of $[***] per kilogram; and (ii) the form of ErgoD2 Water at an initial cost of $[***] per gallon.


(b) Payment terms shall be [***] days after receipt of orders.

(c)  Prices subject to annual review and price adjustment to cover increases in price of raw materials.  Adjusted price increase not to exceed the actual labor and raw material price increases.

(d) Licensee will provide to Licensor, on a quarterly basis, a rolling 12 months’ forecast of estimated purchase requirements for the Compound.

(e) Licensor shall produce and deliver, on an “FOB - Licensor’s production facility” basis,  to Licensee ordered quantities to Licensee’s designated location within the continental U.S. within 30 days of receipt of Licensee’s order.

(f) The term of the contract for sales shall run contemporaneously with this Agreement.

6. Escrow:

(a) Licensor will at all times maintain an adequate supply of Compound to satisfy a six-month production forecast of estimated purchases.  Licensor will promptly provide to Licensee, at Licensee’s reasonable request, written confirmation that Licensor has an adequate supply of Compound to satisfy a six-month production forecast of estimated purchases.

(b) Information about formulas, processes, supplier information and Method of Production for the Compound to be held in escrow by a neutral, third party agreed to by the Parties.  Upon failure of Licensor to deliver the Compound ordered by licensee within a 60-day period, formulas, processes, and supplier information will be provided to licensee with license to practice the Technology to prepare the Compound.

7. Transfer of Certain Assets:

In the event that Licensor owns any personal property related to the Products, including inventory, unfilled bottles, unused labels and the like, the Parties agree in good faith to negotiate for the sale of such assets from the Licensor to the Licensee at no more than cost of production of these items.

8. Confidentiality:

(a) The Parties agree to treat as confidential any and all Confidential Information obtained from each other and to that end further agree that information disclosed pursuant to this Agreement relating to the Formulations, including efforts to commercialize the Formulations, shall be deemed Confidential Information.  Notwithstanding the foregoing, confidential information may be disclosed to the extent required by any law or regulation of any governmental authority having jurisdiction over any of the Parties, with appropriate efforts made to maintain confidentiality.  Both Parties shall maintain Confidential Information in confidence as set forth herein, however, the confidentiality of specific Confidential Information may be maintained for such finite period of time as the Parties may subsequently agree in writing.  There are no obligations of confidentiality as to specific information (a) which is publicly known at the time of disclosure under this Agreement or becomes publicly known at any time other than through disclosure by the recipient of the information; (b) which is demonstrably known to the recipient of the information prior to its receipt from the disclosure; (c) which is disclosed to the recipient by a third party not under an obligation of confidentiality and independently of the studies contemplated by this Agreement; or (d) for which disclosure has been approved by the mutual written consent of the Parties; or (e) independently developed without access to Confidential Information from the discloser.

9. Accounting:


(a) The Royalties shall be payable no later than [***] days after the end of each calendar quarter.

(b) Licensee shall keep complete and accurate records in sufficient detail to permit Licensor to confirm the accuracy of calculations of all payments made pursuant to Section 4 of this Agreement.  Such records shall be retained by Licensee for no less than a five (5) year period following the year in which any such payments were made.  No more than once per calendar year, Licensor shall have the option to engage at its own expense, an independent certified public accountant reasonably acceptable to Licensee, to examine, in confidence, such records kept by Licensee as may be necessary to determine, with respect to any calendar year, the correctness of any payment made pursuant to Section 4 of this Agreement. The report of such accountant shall be limited to a certificate verifying any report made or payment submitted by Licensee during such period but may include, in the event the accountant shall be unable to verify the correctness of any such payment, information relating to why such payment is unverifiable. All information contained in any such certificate shall be deemed to be Licensee’s Confidential Information hereunder. If any audit performed under this paragraph shall indicate that any payment due pursuant to Section 4 was underpaid, Licensee shall pay Licensor the amount of any underpayment promptly.

10. Intellectual Property Rights:

(a) Licensor’s Intellectual Property Rights.  Licensor is the sole owner or rightful licensee of all right, title and interest in and to the Copyrights, Technology, Formulations and Trademarks.  No ownership in any Copyrights, Technology, Formulations and/or Trademarks shall pass to the Licensee by the issuance of the license contained in this Agreement.  The Licensee’s use of Copyrights, Technology, Formulations and Trademarks is authorized only for the specific purposes and to the extent expressly set forth in this Agreement, and upon termination of this Agreement such authorization will cease immediately, subject to the provisions of Section 14(b), and the Licensee will promptly deliver to the Licensor all copies, extracts, summaries and other tangible embodiments of the Copyrights, Formulations and Trademarks which it may have obtained during the Term.  The Licensee has no, and does not and will not claim any, rights in or to any Copyrights, Technology, Formulations and/or Trademarks other than the limited grant of license made by the Licensor herein, and will acquire no additional rights during the Term unless the same are expressly granted in a writing signed by both Parties and evidencing separate consideration therefor.

(b) Licensee’s Intellectual Property Rights.  Licensee is the sole owner or rightful licensee of all right, title and interest in and to all of Licensee’s technology, proprietary concepts, ideas and developments related to the design, content, manufacture, marketing, sale and/or distribution of the Articles including, without limitation, those made with the Compound, and all technology, text, images, graphics, data and other information embodied or used therein, and any and all present or future generations, modifications, enhancements, improvements and copies thereof, and in all trademarks, trade names, service marks, trade dress, inventions, copyrights, patents, know-how and trade secrets used in or in connection with the Articles, including any and all of the foregoing which may be discovered, developed, created or obtained during the Term (collectively, the “Licensee’s Rights”).  Licensee’s Rights explicitly shall NOT include the Copyrights, Technology, Formulations and/or Trademarks.  Licensor has no, and does not and will not claim any, rights in or to any Licensee’s Rights, and will acquire no additional rights during the Term unless the same are expressly granted in a writing signed by both Parties and evidencing separate consideration therefor.

(c) No Reverse Engineering.  Licensee shall not reverse engineer or attempt to reverse engineer the Compound or its components during the Term.

(d) In the event a third party shall misappropriate any Copyrights, Formulations and/or Trademarks, Licensee shall give notice of that situation to Licensor, and Licensor shall take action to discontinue such misappropriation.


10A. Dr. Marvin Hausman’s Services:

(a) The parties acknowledge that Licensor currently employs Dr. Marvin Hausman (“Dr. Hausman”) as Licensor’s Chief Science and Technology Officer.

(b) During the Term and within the Territory, Licensor shall cause Dr. Hausman to provide spokesperson and public relations services to Licensee on a non-exclusive basis, which services include, without limitation, interviews and the like, on a quarterly basis during the first year of the Term and on a semi-annual basis thereafter, not to exceed eighteen (18) days in the first year and six (6) days in the second year (“Dr. Hausman’s Services”).

(c) Notwithstanding the foregoing provision, in no event will Dr. Hausman’s Services place an unreasonable burden on Dr. Hausman’s ability to fulfill his responsibilities as Chief Science & Technology Officer of Licensor.

(d) During the performance of Dr. Hausman’s Services, Licensor shall continue to pay Dr. Hausman for his employment as Licensor’s Chief Science and Technology Officer and cover all applicable benefits and insurance, provided that Licensee shall pay any and all pre-approved expenses of Dr. Hausman reasonably related to Dr. Hausman’s Services including, but not necessarily limited to, travel, lodging and sustenance.

(e) Upon Licensee’s request, Licensor shall cause Dr. Hausman to enter into a written agreement with Licensee on the terms set forth in this Section 10A.

11. Conditions Precedent and Due Diligence:

(a) Each and every obligation of Licensee to be performed under this Agreement shall be subject to the satisfaction prior to or on the Closing Date of the following conditions:

(i) The contract for sales of the Compound referenced in Section 5.

(ii) Licensee shall have completed Due Diligence Investigation to Licensee’s complete satisfaction; and

(iii) Compliance with the insurance requirements set forth in Section 13(d).

(b) Licensee shall have until April 1, 2017 (“Due Diligence Period”) to perform a reasonable investigation into the Copyrights, Formulations, Technology (outside of those Technology matters to be retained in escrow) and Trademarks (the “Due Diligence Investigation”).  The Due Diligence Period may be extended by the mutual written agreement of the Parties.  The date on which the Due Diligence Period ends is referred to as the “Closing Date”.  If during the Due Diligence Period, Licensee finds any information or conditions concerning the Copyrights, Formulations, Technology and/or Trademarks which are objectionable to Licensee within Licensee’s sole discretion, or Licensee elects for any or no reason whatsoever not to proceed with this Agreement, Licensee may terminate this Agreement by written notice to the Licensor delivered prior to the end of the Due Diligence Period.  For the avoidance of doubt, in the event that Licensee elects to not proceed with this Agreement on or before the Closing Date, Licensee is not obligated to pay Licensor the amount set forth in Section 4(a)(ii) hereunder.

(c) No later than ten (10) business days after the Effective Date, Licensor shall provide to Licensee the following:


(i) the Formulations.  Where appropriate, Licensor shall identify its trade secrets by appropriate marking of documents containing them, such as the legend “Proprietary” or “Confidential.”  For secrets transmitted orally, Licensor shall communicate similar indications orally;

(ii) samples of the Compound in amounts sufficient to prepare the Existing Products for testing;

(iii) various files for the production of Existing Products in electronic format to be determined in Licensee’s reasonable discretion, including labels, marketing materials and the like;

(iv) a list of personal property related to the Products, including inventory, unfilled bottles, unused labels and the like; and
(v) pertinent licenses, title documents and other information and documentation pertaining to the Copyrights, Formulations, Technology (outside of those Technology matters to be retained in escrow) and Trademarks.
 
 (b) During the Due Diligence Period, without cost to Licensee, Licensor shall assist and consult with Licensee or its designee upon reasonable request on any topic reasonably related to the Formulations, including formulation components other than those related to production of the Compound, formulating methods, manufacturing methods, plant identification, plant medicinal properties, sourcing of plant materials, information from users regarding safety, efficacy, and side effects, including anecdotal information, and any information useful in establishing a clinical study.
 

12. Warranties and Representations:

(a) The Parties hereby make the representations and warranties set forth below, as to such Party only, which representations are true and correct as of the Effective Date, and if any of such representations or warranties become untrue or materially misleading throughout the Term, the Party making such representation or warranty shall notify the other of such fact promptly upon becoming aware thereof:

(i) such party has all necessary rights and authorizations to enter into and perform this Agreement in accordance with its terms, and each person signing this Agreement for and on behalf of such party has the full corporate power and authority to execute and deliver this Agreement for and on behalf of such party, which Agreement, once so executed and delivered, will be the legally binding obligation of such party, enforceable against it in accordance with its terms;

(ii) nothing in this Agreement will cause such party to be in breach or violation of any: (A) law, regulation or court or administrative order to which such party is subject, or (B) provision of its organizational charter documents, or (C) material provision of any contract, arrangement, undertaking or understanding to which such party is a signatory, or by which its properties or assets is bound;

(iii) there is no demand, claim, suit, action, arbitration, or other proceeding, pending or, to the knowledge of such party, threatened, that questions or challenges the ability or right of such party to enter into this Agreement or to perform any of its obligations hereunder; and

(iv) each party is the lawful owner, or rightful licensee, of any and all technologies, proprietary rights and Confidential Information which it may grant, provide to, or deliver to the other party hereunder, free and clear of all encumbrances, charges, liabilities and obligations, and such technologies, proprietary rights and Confidential Information do not infringe, to the best of Licensor’s knowledge, upon the U.S. registered patent rights, or other intellectual property rights, of a third party.  The sharing or delivery of such items of technology, proprietary information and/or Confidential Information in the manner contemplated by this Agreement shall not infringe upon any third-party rights.


(b) Without limiting the generality of the foregoing, Licensor hereby makes the representations and warranties set forth below, as to Licensor only, which representations are true and correct as of the Effective Date, and if any of such representations or warranties become untrue or materially misleading throughout the Term, Licensor shall notify Licensee of such fact promptly upon becoming aware thereof:

(i) The Compound and the Existing Products are safe for the treatment of hair, skin and anti-aging;

(ii) Product claims made by Licensor on the Existing Products are true and correct;

(iii) The technologies, proprietary rights and Confidential Information granted, provided to and/or delivered by Licensor to Licensee hereunder are sufficient for Licensee’s use of the Compound in the Fields of Use including, without limitation, in the production of the Existing Products;

(iv) Licensee is the lawful owner, or rightful licensee, of the Patents, free and clear of all encumbrances, charges, liabilities and obligations;

(v) The Method of Production and the Formulations constitute “trade secrets” as such term is defined in 18 U.S.C. § 1839; and

(vi) Licensee is the lawful owner, or rightful licensee, of the Method of Production and other trade secrets, free and clear of all encumbrances, charges, liabilities and obligations; and the Method of Production does not infringe, to the best of Licensor’s knowledge, upon the U.S. registered patent rights, or other intellectual property rights, of a third party.

13. Indemnification and Insurance:

(a) Each Party (the “Indemnifying Party”) shall indemnify and hold the other Party and its officers, directors, principals, partners, employees, agents and representatives (each an “Indemnified Party”) harmless for, from, and against any and all losses, damages, liabilities, claims, suits, expenses and all other costs of any type, including reasonable attorneys’ fees (collectively, “Damages”), and shall reimburse each Indemnified Party for all Damages insofar as they result from, arise in connection with, or are related in any way to: (i) any breach by the Indemnifying Party of its representations, warranties, agreements or obligations hereunder;  (ii) any intentional or negligent act of omission or commission by the Indemnifying Party; (iii) the acts or omissions of the Indemnifying Party which are alleged to have caused any loss, property damage, personal injury, or death to any individual or entity; (iv) any claim, action or proceeding brought against Licensee or any affiliate that any Compound, Copyright and/or Formulation, or Trademark provided hereunder infringe any known or unknown patent, copyright, trademark, trade secret or other intellectual property rights of a third-party; or, (v)  the failure of Licensor to comply with the laws, rules, regulations, ordinances, statutes, codes and orders of any governmental or quasi-governmental or regulatory or administrative authority.  This Section 13(a) does not in any way limit any Party’s rights against the other for any breach of this Agreement, which remedies are cumulative and non-exclusive.
 
 (b) The foregoing indemnities will be provided, subject to the Indemnifying Party (a) promptly notifying the Indemnified Party in writing of the claim; and (b) allowing the Indemnifying Party to control the defense and reasonably cooperating with the Indemnifying Party in the defense and any related settlement negotiations, with the Indemnified Party having the right to approve any such settlement.


(c) During the Term, the Parties shall maintain general insurance of at least $1,000,000 per occurrence and $2,000,000 in aggregate, listing the other Party as an additional insured.  Within thirty (30) days after the Effective Date and thereafter annually between January 1 and January 31 of each year, each Party shall present evidence to the other Party that the coverage is being maintained as required above.  Each Party shall provide the other Party with at least thirty (30) days prior written notice of any change in or cancellation of the insurance coverage.

14. Termination:

(a) This Agreement may be terminated by either Party:

(i) at any time upon the material breach by the non-terminating Party of any agreement, covenant, representation or warranty contained herein, provided that the breaching Party shall have thirty (30) days in which to cure such breach to the non-breaching Party’s complete satisfaction (to the extent such breach is of a type which is capable of being cured);

(ii) immediately by the upon any notice of the insolvency, moratorium or assignment for the benefit of creditors, or the filing of any voluntary or involuntary petition for bankruptcy by or against the non-terminating Party.

(b) Without limiting the generality of the foregoing, this Agreement may be terminated by Licensor if Licensee fails to meet the yearly minimum Royalties set forth in Section 4(c), provided that, upon any such termination of this Agreement, Licensee shall have six (6) months to fulfill existing orders for Articles.

(c) Without limiting the generality of the foregoing, this Agreement may be terminated by Licensee:

(i) If total revenues based on gross invoiced sales of Articles during the first three (3) years of the Term fail to reach $[***], then Licensee may either: (i) terminate the Agreement; or (iii) reduce the minimum yearly Royalties to [***]% of Net Sales, provided that such Royalties will be paid until total revenue based on gross invoiced sales of Articles equal [***].

(ii) Without fault of Licensee or its employees, agents, or consultants, the Formulations become generally known in the Fields of Use;

(iii) The Formulations are disclosed by Licensor to a third party without obligation of confidence;

(iv) The Copyrights, Patents and/or Trademarks are rejected, denied, cancelled and/or otherwise invalidated;

(v) The Method of Production is disclosed by Licensor to a third party without obligation of confidence; and/or

(vi) Any of Licensee’s representations and warranties as set forth in Section 12(b) become untrue or materially misleading at any time during the Term.


(d) Except as otherwise specified herein, termination of this Agreement by either Party for any reason shall not relieve either Party of its duties owed to the other Party pursuant to the terms hereof, including without limitation the payment of all accrued but unpaid License Fees, where such Party’s duty arises out of its obligations to perform hereunder at any time prior to the effective date of such termination and including duties of confidentiality.

(e) Except as otherwise specified herein, termination under this Section does not in any way limit any Party’s rights against the other for any breach of this Agreement, which remedies are cumulative and non-exclusive.

15. Miscellaneous:

(a) All notices required or permitted to be given hereunder shall be in writing and sent by personal delivery, by facsimile or electronic scan, by overnight courier or by first class mail, registered or certified, postage prepaid with return receipt requested, addressed to the other Party at the address provided in the preamble to this Agreement, or to such other address as either Party may hereafter designate to the other in writing pursuant to this Section 15(a).  A notice under this Agreement will be effective on the date of personal delivery, or of delivery by facsimile or electronic scan (if verification of actual or electronic receipt can be provided), the next business day if sent by overnight courier, or three (3) business days after deposit in the U.S. mail.

(b) All payments hereunder shall be made via wire, corporate check or ACH.

(c) No waiver by either Party of default for any obligation of the other Party hereunder shall operate as a waiver in the case of any subsequent default by first Party.

(d) All monetary amounts are in United States dollars.

(e) The Parties agree that this Agreement will be understood to be in force under the laws of the State of New York.  In the event of a dispute arising under this Agreement, the Parties agree to meet in good faith to resolve the dispute. If such efforts are unsuccessful, the parties shall submit the dispute to non-binding mediation before a neutral mediator in New York prior to any lawsuit. The Parties consent to jurisdiction in the state and federal district of Southern District of New York in the event of a lawsuit.

(f) No other promise or written agreements will be permitted to change any of the terms of this Agreement, except and only to the extent that such changes result from subsequent written amendments agreed to and signed by both Parties.

(g) This Agreement may be executed in counterparts, each of which shall be deemed an original, but all of which together shall constitute one and the same instrument.  A signed copy of this Agreement transmitted by facsimile, email or other means of electronic transmission shall be deemed to have the same legal effect as delivery of an original executed copy of this Agreement for all purposes.

(h) This Agreement sets forth the entire agreement between the Parties pertaining to the subject matter hereof and supersedes all negotiations, preliminary agreements, memoranda or letters of proposal or intent, discussions and understandings of the Parties.  All discussions between the Parties have merged into this Agreement, and neither party shall be bound by any definition, condition, understanding, representation, warranty, covenant or provision other than as expressly stated in or contemplated by this Agreement or as subsequently shall be set forth in writing and executed by a duly authorized representative of the Parties to be bound thereby. No amendment or modification of this Agreement shall be valid or binding upon the Parties, unless agreed upon by the Parties, made in writing, and signed on behalf of the Parties by their duly and legally authorized representative officers.

(i) If either party brings legal action to enforce its rights under this agreement, the prevailing party will be entitled to recover its expenses (including reasonable attorneys’ fees) incurred in connection with the action and any appeal.


IN WITNESS WHEREOF, the undersigned are duly authorized to execute this Agreement on behalf of Licensee and Licensor.

_____________________________________
Entia Biosciences, Inc.
By: _________________________________
Title: ________________________________
Date: ________________________________
_____________________________________
GROH BEAUTY CORP
By: _________________________________
Title: ________________________________
Date: ________________________________

SCHEDULE A
[Copyrights]
 
 
 
 
 
 
 
 


SCHEDULE B
[Existing Products]

1. GROH Ergo Boost Daily Replenishing Supplement

2. GROH Ergo Boost Hair & Scalp Conditioning Treatment

3. GROH Ergo Boost Skin Repair Treatment

4. GROH Ergo Boost Skin Recharging Bar

5. GROH Ergo Boost Professional Series-Hair & Scalp Treatment

SCHEDULE C
[Patents]

1. US Patent Application 20140363379 - Hair, Skin and Nail

2. US Patent 8492106 B2


SCHEDULE D
[Trademarks]

1. THE BEAUTY OF WELLNESS - Reg. No. 4,703,565

2. CREATED BY NATURE, UNLOCKED BY THE SCIENCE - Reg. No.4,418,247

3. ERGOD2 - Reg. No 4,303,969

4. ERGO ESSENCE - Reg. No.  4,456,779

5. GROH ERGO   Boost” Reg. No. 4,501,187

6. GROH - Reg. No. 4,262,769

7. ORGANIC IS NOT ENOUGH - Reg. No. 4,495,008

8. UNLOCK YOUR INNER POWER TO GROH - Reg. No. 4,428,931.

EX-99.3 4 ex99-3.htm EX-99.3
 
EXHIBIT 99.3
 
Pursuant to 17 CFR 240.24b-2, confidential information has been omitted in the places marked ‘[***]’ and has been filed separately with the Securities and Exchange Commission pursuant to a Confidential Treatment Application filed with the Commission.


CONTRACT FOR THE SALE OF GOODS

This CONTRACT FOR THE SALE OF GOODS (the “Agreement”) is dated as of the date of the last signature below (the “Effective Date”), by and between Entia Biosciences, Inc. of 13565 SW Tualatin-Sherwood Rd. Suite 800, Sherwood, Oregon 97140 (“Seller”) and GROH BEAUTY CORP of 508 SW 12th Avenue, Deerfield Beach, Florida 33442 (“Buyer”).  Seller and/or Buyer are sometimes individually referred to as a “Party” and collectively as the “Parties”.

WHEREAS, the Parties have or will enter into that License Agreement, on or around the same date as the Effective Date;

WHEREAS, the License agreement obligates the Parties to negotiate in good faith for a contract for sales of the Compound having certain material terms; and

WHEREAS, the Parties intend to memorialize certain material terms and other terms in a more formal agreement.

NOW, THEREFORE, for good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, the Parties agree as follows:

1. Certain Definitions Incorporated:

The Parties hereby incorporate by reference the definitions of “Compound”, “Term” and “Territory” as such terms are defined in the License Agreement.  Seller shall not change the composition of the Compound without prior agreement in writing between the parties.  Except changes made or directed by regulatory agency, law or resulting from issues arising related to safety.

2.  Sale of Goods: 

(a) During the Term and within the Territory, Subject to the Price Adjustment set forth below, the Seller shall sell to the Buyer and the Buyer shall purchase from the Seller the goods set forth on Exhibit A (the “Goods”) in the quantities and at the prices stated in Exhibit A.  Seller’s obligations to sell the Goods to Buyer are on a non-exclusive basis.

(b) Unless otherwise stated in Exhibit A, the Buyer shall pay all taxes and third-party expenses imposed on, in connection with, or measured by the transaction contemplated by this agreement in addition to the prices set forth on Exhibit A.

(c) The prices set forth in Exhibit A are subject to Seller’s annual review and price adjustment to cover increases in price of raw materials, provided that the adjusted price increase will not exceed the actual labor and raw material price increases (the “Price Adjustment”).  Price changes are effective no earlier than thirty (30) calendar days after Seller’s communication of such changes to Buyer.  Price changes do not affect Buyer’s orders on or before this date to the extent that buyer’s order do not reflect an effort to “pipeline fill” for the purpose of avoiding the price increase.  “Pipeline fill” will be reflected in orders that significantly increase order quantities compared to order activity from the last 90 days and / or a significant deviation from quantites forecasted by the buyer according to the provisions in Section 5 (d) of the License Agreement.


(d) Buyer may send purchase orders to Seller electronically at an email address to be provided to Buyer upon Buyer’s reasonable request.

3.  Invoices; Payment: 

(a) Unless otherwise stated in Exhibit A, payment for the Goods is due within [***] of the date of the Seller’s receipt of Buyer’s order.  All payments hereunder shall be made via wire, corporate check or ACH.  All monetary transactions will be in U. S. Dollars ($).

(b) The Buyer shall pay a delinquency charge of the greater of [***]% per month and (2) the highest rate allowed under applicable law on all overdue amounts until the amounts are paid.

4.  Delivery; Title; Risk of Loss; Shipping Costs:

(a) Seller shall produce and deliver, on an “FOB – Seller’s production facility” basis, to Buyer ordered quantities of the Goods to Buyer’s designated location within the continental U.S. within 30 days of receipt of Buyer’s order, and title to and risk of loss of the Goods will pass to the Buyer upon such delivery by the Seller.

(b) Buyer shall be responsible for all shipping costs.

(c) All Goods will be packaged in accordance with Buyer’s reasonable instructions received by Seller prior to delivery and Seller shall pay all reasonable costs of packaging.

(d) Seller hereby acknowledges and agrees that all Goods must fully conform to this Agreement and failure of Seller to adhere to any portion of this Agreement including, without limitation, quantity, quality, and time of performance, shall constitute a material breach of this Agreement.  Without limiting the generality of the foregoing, time of delivery is of the essence.

5. Right of Inspection; Returns:

(a) Buyer has the right to inspect the Goods upon receipt and has 14 days in which to notify seller of any claim for damages based on the condition, grade, quantity or quality of the Goods. Such notice must specify in detail the particulars of the claim. Failure to provide such notice within the requisite time period constitutes irrevocable acceptance of the Goods.

(b) Buyer may return Goods that are nonconforming for a cash refund.

6. Forecast of Estimated Purchase Requirements:

Buyer shall provide to Seller, on a quarterly basis, a rolling 12 months’ forecast of estimated purchase requirements for the Goods.

7.  Warranties and Representations; Indemnity:

(a)
Seller warrants that:


(i) the Goods are free from any and all security interests, liens, and encumbrances; and

(ii) the Goods do not infringe, to the best of Seller’s knowledge, upon the U.S. registered patent rights, or other intellectual property rights, of a third party.

(b) If a claim or allegation is brought against the Buyer that the Goods created by Seller infringes on any third party’s intellectual property rights, the Seller agrees to and shall defend, indemnify and hold Buyer harmless from and against such claim or allegation, including reimbursing Buyer for all legal fees and expenses incurred in the investigation and defense of such claim or allegation and any royalties, payments, damages, penalties and interest that may be awarded therein or agreed to by Seller.  As a condition of the foregoing, Buyer may agree to allow Seller, at Buyer’s option to either procure the necessary rights to allow Buyer to continue use of the Goods created by Seller or to replace or modify the Goods until it is deemed to be non-infringing.  Seller shall have no obligation or liability whatsoever for any claim of infringement solely based upon work or materials provided by Buyer or any third party (other than third party materials that are part of Seller’s Goods), or for any claim of infringement based solely on Buyer’s modification of the Goods provided by Seller.

8.  Governing Law and Designation of Forum:

The Parties agree that this Agreement will be understood to be in force under the laws of the State of New York.  In the event of a dispute arising under this Agreement, the Parties agree to meet in good faith to resolve the dispute. If such efforts are unsuccessful, the parties shall submit the dispute to non-binding mediation before a neutral mediator in New York prior to any lawsuit. The Parties consent to jurisdiction in the state and federal district of Southern District of New York in the event of a lawsuit.

9.  Force Majeure:

Notwithstanding any other terms and conditions of this Agreement, in the event that either Party is materially unable to perform any of its obligations hereunder because of natural disasters, Acts of God, riots, wars, acts of terrorism, governmental action or any other event, whether or not similar to the causes specified herein that are beyond such Party’s control, then such Party shall, upon written notice to the other Party, be relieved from its performance of such obligations solely to the extent and for the duration that such performance is prevented by such events, provided that such Party shall at all times use its best efforts to resume such performance.

10.  Assignment; Delegation: 

Neither Party may assign any of its rights under this agreement or delegate any performance under this agreement, except with the prior written consent of the other Party. Any purported assignment of rights or delegation of performance in violation of this section is void.

11.  Recovery of Expenses: 

In any adversarial proceedings between the parties arising out of this agreement or the transactions it contemplates, the prevailing party will be entitled to recover from the other party, in addition to any other relief awarded, all expenses that the prevailing party incurs, including legal fees and expenses.

12.  Entire Agreement: 

This Agreement and the License Agreement constitute the entire agreement between the parties with respect to the subject matter of this Agreement and supersedes all other agreements, whether written or oral, between the parties.  In the event of any conflict, ambiguity or inconsistency between or among this Agreement and the License Agreement, the terms and conditions of this Agreement shall control.


13.  Amendments: 

No amendment to this agreement will be effective unless it is in writing and signed by both parties.

14.  Counterparts; Electronic Signatures:

This agreement may be signed in one or more counterparts, which together will form a single agreement. This agreement may be signed electronically.


IN WITNESS WHEREOF, the undersigned are duly authorized to execute this Agreement on behalf of Buyer and Seller.


_____________________________________
Entia Biosciences, Inc.
 
By: _________________________________
 
Title: ________________________________
 
Date: ________________________________
_____________________________________
GROH BEAUTY CORP
 
By: _________________________________
 
Title: ________________________________
 
Date: ________________________________



EXHIBIT A
 
Goods
Price
The Compound in the dry powder form of ErgoD2
$[***] per kilogram
The Compound in the form of ErgoD2 water
$[***] per gallon



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