-----BEGIN PRIVACY-ENHANCED MESSAGE----- Proc-Type: 2001,MIC-CLEAR Originator-Name: webmaster@www.sec.gov Originator-Key-Asymmetric: MFgwCgYEVQgBAQICAf8DSgAwRwJAW2sNKK9AVtBzYZmr6aGjlWyK3XmZv3dTINen TWSM7vrzLADbmYQaionwg5sDW3P6oaM5D3tdezXMm7z1T+B+twIDAQAB MIC-Info: RSA-MD5,RSA, O08Jq7ZFC/seiRVMu0SkSd7RT42jKIhy8IUO/QvXbmMm84FEzdtH6nhDaIdq89e2 IN/9iJx22F/grBS3xWPDzg== 0001144204-10-034707.txt : 20100623 0001144204-10-034707.hdr.sgml : 20100623 20100623170026 ACCESSION NUMBER: 0001144204-10-034707 CONFORMED SUBMISSION TYPE: 8-K PUBLIC DOCUMENT COUNT: 4 CONFORMED PERIOD OF REPORT: 20100621 ITEM INFORMATION: Entry into a Material Definitive Agreement ITEM INFORMATION: Financial Statements and Exhibits FILED AS OF DATE: 20100623 DATE AS OF CHANGE: 20100623 FILER: COMPANY DATA: COMPANY CONFORMED NAME: IsoRay, Inc. CENTRAL INDEX KEY: 0000728387 STANDARD INDUSTRIAL CLASSIFICATION: SURGICAL & MEDICAL INSTRUMENTS & APPARATUS [3841] IRS NUMBER: 411458152 STATE OF INCORPORATION: MN FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 8-K SEC ACT: 1934 Act SEC FILE NUMBER: 001-33407 FILM NUMBER: 10913141 BUSINESS ADDRESS: STREET 1: 350 HILLS STREET, STREET 2: SUITE 106 CITY: RICHLAND STATE: WA ZIP: 99354 BUSINESS PHONE: (509) 375-1202 MAIL ADDRESS: STREET 1: 350 HILLS STREET, STREET 2: SUITE 106 CITY: RICHLAND STATE: WA ZIP: 99354 FORMER COMPANY: FORMER CONFORMED NAME: CENTURY PARK PICTURES CORP DATE OF NAME CHANGE: 19920703 8-K 1 v188853_8-k.htm Unassociated Document
 


 
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):  June 23, 2010
(June 21, 2010)
 
ISORAY, INC.
(Exact name of registrant as specified in its charter)

Minnesota
(State or other jurisdiction
of incorporation)
001-33407
(Commission
File Number)
41-1458152
(IRS Employer
Identification No.)

350 Hills Street, Suite 106, Richland, Washington 99354
 (Address of principal executive offices) (Zip Code)

(509) 375-1202
(Registrant's telephone number)



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:
 
o
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

o
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

o
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

o
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 
 

 

ITEM 1.01  Entry into a Material Definitive Agreement

On June 21, 2010, IsoRay Medical, Inc. ("Medical"), a wholly owned subsidiary of IsoRay, Inc. (the "Registrant"), entered into a License Agreement (the "Agreement") with Hologic Inc. ("Hologic").  Under the Agreement, Medical received an exclusive worldwide license to Hologic's Gliasite Radiation Therapy System for intracavity radiation therapy of the brain.  The Agreement is terminable upon 90 days prior written notice by Medical or by either party following breach of the Agreement and a 30 day notice and cure period.

On June 23, 2010, the Registrant issued a press release announcing its entry into the Agreement, the text of which is attached hereto as Exhibit 99.1.

ITEM 9.01  Exhibits

 
(c)
Exhibits

10.59
License Agreement, dated effective June 14, 2010, by and between IsoRay Medical, Inc. and Hologic Inc. (confidential treatment requested for redacted portions)

 
99.1
Press release, dated June 23, 2010

SIGNATURES

In accordance with 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.

Dated:  June 23, 2010


 
IsoRay, Inc., a Minnesota corporation
       
 
By:
   /s/ Dwight Babcock
 
   
 Dwight Babcock, CEO
 

 
 

 
 
EX-10.59 2 v188853_ex10-59.htm Unassociated Document
 

License Agreement
for
HOLOGIC, Inc. and ISORAY MEDICAL, Inc.

 
This License Agreement (“Agreement”) is effective as of June 14, 2010 (“Effective Date”), by and between Hologic Inc. (“Licensor”) of 35 Crosby Drive, Bedford MA 01730 and IsoRay Medical, Inc. (“Licensee”) of 350 Hills Street, Suite 106 Richland, WA 99354 (together the “Parties”).

1.   Scope.

WHEREAS Licensor is the owner of the certain Intellectual Property ("Licensor IP"), including technology, know-how, copyrights, patents and trademarks associated with the Gliasite® Radiation Therapy System (excluding the radioisotope(s) used by Licensee in the Gliasite® Radiation Therapy System, the “Product”), including but not limited to the patents identified in Appendix A attached hereto, together with any and all divisions, continuations, reissues, and foreign counterparts (the “Patents”), and the trademarks, service marks, and/or trade names identified in Appendix B hereto including all applications, registrations, renewals, and foreign counterparts thereof, as well as all associated goodwill and other rights at common law (the “Marks”).

WHEREAS Licensee desires to license the Licensor IP for use in the production, manufacture, marketing, promotion, distribution and sale of the Product throughout the world (“Territory”).

WHEREAS Licensor is willing to grant Licensee rights to the Licensor IP in the Territory with a limited field of use of intracavity radiation therapy (brachytherapy) of the brain (“Exclusive Field of Use”); and

WHEREAS, the parties agree that it is desirable to have this Agreement between them, which will govern the license and the use of the Licensor IP.

2.   License.

(a)   License Grant.  Subject to payment of the applicable fees set out below, Licensor hereby grants to Licensee a limited, perpetual, exclusive, assignable, license to use, distribute, and copy Licensor IP as necessary for purposes of internal development, manufacture, distribution, marketing, promotion, and sale of the Product in the Exclusive Field of Use.

(1). Sublicenses: Provided Licensee remains responsible for payment of the fees set forth below, Licensee may sublicense the Licensor IP, as necessary for global manufacture, sale, distribution, marketing and promotion of the Product, to its subsidiaries, manufacturing partners (including outsourcers), distributors, wholesalers, and retailers (“Sublicensees”) with which Licensee has written agreements that, at a minimum, (i) obligate Sublicensees to abide by the License Grant restrictions and the provisions of this Agreement pertaining to the Exclusive Field of Use, export controls and compliance with applicable law, (ii) require Sublicensees to maintain accurate records of Product sales and to provide same to Licensor upon request, and (iii) grant Licensor the rights and standing as a third-party beneficiary of such agreements with the authority to enforce same.
 
Sheet 1 of 7

 
(2). Licensor Retained Rights for Recovery for Infringement: Licensor shall have the right, but not the obligation, exercisable in its sole discretion, to prosecute any claims against third parties for infringement of the Licensor IP and retain any damages recovered as a result (with no duty to share or apportion such amounts with Licensee).  If necessary, in Licensor’s opinion, Licensor may join Licensee as a co-plaintiff in any such claim, suit, action, or proceeding; Licensee shall bear its own costs thereof and shall be entitled to a share of any damages recovered proportionate with Licensee’s costs, versus Licensor’s costs, incurred in the joint prosecution.  If Licensor elects not to prosecute, or to continue prosecuting, any such claim, suit, action, or proceeding, Licensor will give prompt notice thereof to Licensee, and Licensee may prosecute, or continue prosecuting, such claim, suit, action, or proceeding, at is own expense, in which case Licensee, not Licensor, shall be entitled to retain any damages recovered as a result (with no duty to share or apportion such amounts with Licensor).

(3) Equitable Relief: The Parties acknowledge and agree that irreparable injury will result if this Agreement is breached as a result of Licensee’s use, distribution, manufacture, marketing, promotion or sale of the Product to third parties for use in other fields of brachytherapy besides brain brachytherapy, and in particular breast brachytherapy, and that in the event of any actual or potential breach Licensor will have no adequate remedy at law and shall be entitled to seek immediate temporary injunctive or other relief, without the necessity of showing actual monetary damages, subject to hearing as soon as thereafter possible and without granting any time for cure that may be provided in this Agreement. Nothing herein shall be construed as prohibiting any Party from pursuing any other remedies available to it for such breach or threatened breach, including the recovery of damages that it is able to prove.

(b)   Restrictions.  Licensee shall not (i) permit any other entity (including any parent, subsidiaries, affiliated entities, or third parties) to use the Licensor IP without payment of the applicable fees.  Licensee shall not delete or modify the trademark notice applicable to the Marks and shall include same on all marketing and promotional materials created by Licensee.  Licensee shall inform Licensor immediately of any infringement or misuse (including, without limitation, any adoption, use, or registration of a trademark, service mark, or trade name similar to the Marks in the Territory) and cooperate with Licensor, at Licensor’s expense, in its investigation or legal proceeding or action that Licensor pursues to protect its rights in the Marks.  Licensee shall not (i) register or attempt to register, during or after the term of this Agreement, any name, mark, or designation used by Licensor anywhere in the world (or any name, mark, or designation similar thereto), (ii) contest, or assist others in contesting, Licensor’s ownership of the Marks, (iii) incorporate any Marks into Licensee’s trademarks, service marks, company names, Internet addresses, domain names, or any other similar designations, or (iv) use Marks in any way that may cause dilution, tarnishment, or confusion or affect the validity of Marks or that may prove derogatory to Licensor’s name or goodwill. Licensee shall include the applicable trademark notice on all Products and materials bearing the Marks and a legend with any publication (online or other) indicating that the Marks are owned by Licensor.

(c)   Proprietary Rights.  Except for the rights granted above, Licensor retains all rights, title, and interest in and to the Licensor IP, including any improvements thereon or modifications or enhancements thereto (other than the Products), and the absolute and exclusive right, exercisable in Licensor’s sole discretion, to file any divisions, continuations, reissues, and/or foreign counterparts thereof to any Patents.  All use of the Marks hereunder shall inure to the benefit of Licensor.
 
Sheet 2 of 7

 
(d)   Export Regulations.  Licensee agrees that it will not, and will not permit, export, or re-export, directly or indirectly, the Products in violation of the U.S. Export Administration Act, Trading with the Enemy Act, International Emergency Economic Powers Act, and their regulations, or into any country prohibited by an U.S. embargo list (collectively, “Export Regulations”), nor will Licensee use, nor permit use of, the Product for any purpose prohibited by Export Regulations. Licensee will obtain any license(s) that may be required for export, re-export, or use of the Product outside of the United States and shall bear any associated fees, taxes, or charges.

(e)    Quality Assurance.  The quality of Licensee’s Products shall exceed or remain consistent with the reputation that Licensor has established with respect to its product line immediately prior to the Effective Date.
 
3.   Commercial Terms.

(a)   Fees.  In consideration of the above License Grant, Licensee shall pay to Licensor a royalty of [**] of the [**] sale price ([**]) per Product sold or used by Licensee.  For the purposes of the foregoing, a Product shall be considered “sold” or “used” when (i) Licensee [or Sublicensee] has billed the purchaser therefore or (ii) when Licensee [or Sublicensee] has removed a unit of Product from inventory and distributed either to an external or internal user.

(b)   Reports.  No later than 30 days after the end of each calendar quarter, Licensee shall provide a written report to Licensor detailing the number of Products sold or used by Licensee [and Sublicensees] for the applicable reporting quarter and an accounting of the applicable royalty payments thereto.  Such report will show only net quantity, reflecting adjustment for returns of any kind to Licensee during the period reported, identifying the total number of Products sold on a distributor-by-distributor basis. Licensee [and Sublicensees] shall furnish to Licensor, at Licensor’s request, periodic forecasts, budgets, and promotional schedules for marketing and sales of the Product.

(c)   Payment Terms.  Royalties shall be paid within thirty (30) days of the end of each calendar quarter.  Any sum not paid when due shall bear interest on the unpaid balance at the highest rate permitted by law or [**] per month, whichever is lower.  License fees are exclusive of applicable federal, state, and local taxes, tariffs, customs, and duties.

(d)   Audit.  During the term of this Agreement, Licensee shall maintain accurate records regarding its sale of the Product.  Upon reasonable prior written notice, Licensor shall have the right to audit these records during normal business hours. If Licensor’s audit discloses an underpayment of any fees due and owing to Licensor, Licensee shall immediately pay the amount due and owing; where the underpayment was fifteen percent (15%) or more of the amount that should have been paid to Licensor, Licensee shall also reimburse Licensor for the cost of the audit.
 
____________________
[**]Certain information in this document has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.
 
Sheet 3 of 7

 
4.   Confidentiality.

(a)   Confidential Information.  During the term of this Agreement, one party (the “Discloser”) may provide the other party (the “Recipient”) with information the Discloser has identified as “confidential” or “proprietary” (“Confidential Information”).

(b)   Confidential Protection.  Except as expressly permitted in writing, Recipient agrees (i) not to reveal the Confidential Information to any third parties, except to Recipient’s employees, contractors, subcontractors or Sublicensees who have a need to know and have written obligations with Recipient to protect Confidential Information, and (ii) to take precautions, which shall be at least the more protective of (A) reasonable and prudent care or (B) those taken in safeguarding its own trade secret, confidential, or proprietary information, whether by instruction, agreement, or otherwise, to satisfy its obligations under this Agreement with respect to authorized use, protection, and security of the Confidential Information.

(c)   Restrictions.  The foregoing restrictions do not extend to information that (i) is at the time of disclosure already known to Recipient from a source not under a confidentiality obligation, (ii) is publicly known at the time of its disclosure through no wrongful act or breach of any obligation of confidentiality, (iii) is published or otherwise made known to the public by Discloser, or (iv) is received by Recipient from a third party who is not bound by any confidentiality obligations with respect to such information.

(d)   Mandatory Disclosure.  In the event Recipient is requested or required by legal process to disclose any Confidential Information, Recipient shall give prompt advance notice so that Discloser may seek a protective order or other appropriate relief.  In the event that such protective order is not obtained, Recipient shall disclose only that portion of Confidential Information that its counsel advises it is legally required to disclose, provided that Recipient shall exercise its reasonable efforts to preserve confidentiality of Confidential Information including, without limitation, by cooperating with Discloser to obtain an appropriate order or other.

(e)   Injunctive Protection.  Recipient agrees that the wrongful disclosure of Confidential Information will cause Discloser irreparable injury that is inadequately compensable in monetary damages.  Accordingly, Discloser shall be entitled to injunctive relief in any court of competent jurisdiction for the breach or threatened breach of this Section, in addition to any other remedies at law or equity.

5.   Warranty.

Licensor warrants, (a) that it is the owner of the Licensor IP with full, free, clear, and unencumbered right to grant the License herein; (b) that the License does not violate the terms of any agreement between Licensor and a third party pertaining to the Licensor IP; and (c) that, to its knowledge, the Patent does not infringe upon any other patent. The above warranties are limited warranties and the only warranties made by Licensor.  To the extent permitted by law, Licensor disclaims all other warranties, express or implied, including (without limitation) the warranties of merchantability and fitness for a particular purpose.
 
Sheet 4 of 7

 
6.   Indemnity

(a)   By Licensor.  Licensor shall defend Licensee, and indemnify same against damages finally awarded as the result of, third-party claims that use of the Patents violates such third party’s valid patent rights, provided Licensee gives Licensor (i) prompt written notice of such claim, (ii) sole control of the defense and/or settlement of such action, and (iii) full cooperation with such defense.  Licensor shall have no liability for any claim of infringement based in whole or in part on use of the Patents outside the scope of its claims or use or combination of the Patents with other technology or materials.  If a third party’s claims substantially interfere with, or Licensor believes that a third-party claim may substantially interfere with, Licensee’s use of Patents, Licensor will, at its sole cost, expense, and selection, obtain a license for Licensee to continue use of the Patent, or [**].

(b)   By Licensee.  Licensee shall defend Licensor, and indemnify same against damages finally awarded as the result of, third-party claims that use of the Product violates such third party’s valid patent rights (except to the extent such claim is based on use of the Patent separately and distinctly from use of the Product), provided Licensor gives Licensee (i) prompt written notice of such claim, (ii) sole control of the defense and/or settlement of such action, and (iii) full cooperation with such defense. This Section shall constitute Licensee’s entire liability and Licensor’s exclusive remedy for such a claim of infringement.

7.   Limitation of Liability.  To the extent permitted by law, and except for obligations under Section 2(c) (Equitable Relief) , Sections 3 (Commercial Terms) or 6 (Indemnity), or for breach of a license grant, neither party will have any liability under this Agreement for: (a) consequential, incidental, exemplary, special, or punitive damages even if advised of the possibility of such (including, but not limited to, loss of business, profits, business information, or business interruption or any other pecuniary loss); or (b) for direct damages, actually proven, exceeding the amounts paid by Licensee for the License the subject of the claim. This limitation shall be enforced even if it causes an exclusive remedy to fail of its essential purpose.

8.   Term and Termination

(a)   Term.  This Agreement shall commence on the Effective Date and shall continue thereafter unless terminated earlier as provided below.

(b)   Termination.

(i)   Licensee may terminate the License at any time upon 90 days prior written notice to Licensor.

(ii)   Either party may terminate this Agreement upon 30 days’ prior written notice if: (a) the other party materially breaches the Agreement and fails to cure the breach within such 30-day period; or (b) the other party files a petition seeking bankruptcy protection, has an involuntary bankruptcy petition filed against it, has a receiver appointed, or otherwise declares its inability to maintain its business or pay its debts as they become due, unless such is dismissed within 90 days of the original filing. Licensee acknowledges and agrees that failure to pay fees, or deliver reports, when due constitutes a material breach of the Agreement.
 
____________________
[**]Certain information in this document has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.
 
Sheet 5 of 7

 
(c)   Rights Upon Termination.  Upon termination of this Agreement:

(i)   Licensee shall immediately cease use of the Licensor IP, in any way (other than for pending unfilled orders made by customers prior to termination), including in production of the Product;

(ii)   Licensee shall provide Licensor with a final report (in the same format as that required by Section 3(b) above) detailing a full count of all Product units in inventory, whether in the possession or subject to the control of Licensee and Sublicensees, or otherwise in existence as of the date of termination, and the applicable royalty fees for such count;

(iii)    Licensee shall terminate all sublicenses granted to Sublicensees for use of the Licensor IP and recover all Licensor Confidential Information from Sublicensees;

(iv)   All amounts then owed shall immediately become due and payable, and each party will cease the use of and return or destroy (and certify the destruction of) all property, including Confidential Information, of the other party in its possession or subject to its control; and

(v)   Licensee shall cease, and shall require Sublicensees to cease, any marketing or representation that Licensee and Sublicensees are licensed to use the Patent in respect of the Product or otherwise.

9.   Assignment.

Licensee may not assign this Agreement or License to anyone without prior written consent, excluding any parent or subsidiary, and excluding as part of the sale of any portion of its business, or pursuant to any merger, consolidation, or reorganization or operation of law.

10.   Governing Law.

This Agreement and performance hereunder shall be governed by the laws of the State of Massachusetts.  Sole venue and jurisdiction for any proceedings under this Agreement shall be in the state and federal courts located in Massachusetts, United States of America.

11.   Force Majeure.

Except for an obligation to pay fees, neither party shall be liable for failure to perform any of its obligations under this Agreement during any period in which such party cannot perform due to matters beyond their control, including, but not limited to, strike, fire, flood, or other natural disaster, war embargo, or riot, provided that the party so delayed immediately notifies the other party of such delay.
 
Sheet 6 of 7

 
12.   Notices.

All notices required or permitted under this Agreement shall be in writing and shall be deemed delivered when delivered in person or deposited in the United States mail, postage prepaid, registered, or certified mail, return receipt requested at the address first set forth above, directed to ‘Attn. Legal Department’ or ‘Attn. Accounting Department’ as appropriate.  Facsimile or electronic signatures shall be deemed equivalent to original signatures for purposes of this Agreement.

13.   Waiver.

The waiver or failure of Licensor to exercise in any respect any right provided for herein shall not be deemed a waiver of any further right hereunder.

14.   Severability.

If any provision of this Agreement is invalid, illegal, or unenforceable under any applicable statute or rule of law, it is to that extent to be deemed modified in order to comply with applicable law, and the remaining provisions shall not be affected in any way.

15.   Entire Agreement and Amendment.

This Agreement constitutes the entire agreement and understanding between the parties and supersedes any prior agreement or understanding whether oral or written relating to the subject matter hereof.  This Agreement may be modified only by a written agreement signed by both parties, and no deletion, additions, or revisions to this Agreement will be valid unless signed by both parties.  The headings used herein are for convenience only and shall not control or affect the meaning or construction of any provisions of this Agreement.


WHEREFORE, the parties have caused their authorized representatives to signify their agreement to these terms by signing below.

/s/ Dwight Babcock
 
/s/ Robert Cascella
ISORAY MEDICAL, INC.
 
LICENSOR SIGNATURE
Printed Name: Dwight Babcock
 
Printed Name: Robert A. Cascella
Title: CEO
 
Title: President, Chief Operating Officer
Sheet 7 of 7

APPENDIX A – LICENSED PATENTS – restricted to field of brain brachytherapy

Docket No.
Title
Serial No.
Patent No.
14.001011 CA
Tumor Treatment (CA)
 
2,068,281
2,068,281 (CA)
14.001011 US PRI
Tumor Treatment
Children:
·     08/727,259
·     09/158,682
·     08/307,165
·     08/818,966
07/715,923
5,429,582
14.001011 US CON
Radiation Treatment of Tumors Using Inflatable Devices
Parent: 5,429,582 (07/715,923)
Children:
·     08/727,259
·     09/158,682
·     08/818,966
08/307,165
5,611,767
14.001011 US DIV 4
Tumor Treatment
Parent: 5,611,767 (08/307,165)
Children: 09/158,682
08/818,966
6,022,308
14.001011 US CON 3
Tumor Treatment
Parent: 6,022,308 (08/818,966)
09/158,682
6,083,148
14.001011 JP
Tumor Treatment
05-500858
3,505,622  Japan
14.001011 EP
Tumor Treatment
92913085.4
0586567 EU
Britain, France,
Germany &Italy
14.001011 JP
Tumor Treatment
No Children
05-500858
3,505,622  Japan
14.002011 US CIP
Inflatable Devices for Tumor Treatment
Parent: 5,611,767 (08/307,165)
Children: PCT/US97/18250
08/727,259
5,931,774
14.002011 JP
“Inflatable Devices for Tumor Treatment
 
ISSUED 7/6/07
3981415
 
A-1

 
14.002011 EP
Inflatable Devices for Tumor Treatment
 
ISSUED 2/09/05
0934094 / Validated in DE, FR, and GB
14.002011 CA
 
“Inflatable Devices for Tumor Treatment
ISSUED 07/29/08, No Children Filed
 
Patent Number 2267958
14.003011 US PRI
Catheter with Permeable Hydrogel Membrane
Children: 09/724,121
09/275,910
6,200,257
14.003011 US CON 1
Catheter with Permeable Hydrogel Membrane
Parent: 6,200,257 (09/275,910)
09/724,121
6,537,194
14.004011 US CIP
Interstitial Brachytherapy Apparatus and Method for Treatment of Proliferative Tissue Diseases
Parent: 5,913,813 (08/900,021)
Children: 09/464,727
09/293,524
6,413,204
14.005011 US CIP
Asymmetric Radiation Dosing Apparatus and Method
Parent: 6,413,204 (09/293,524)
Children: PCT/US00/33613
09/464,727
6,482,142
14.005011 CA
Asymmetric Radiation Dosing Apparatus and Method
2,394,562
2,394,562 (CA)
14.005011 EP
Asymmetric Radiation Dosing Apparatus and Method
 
Patent Number 1239920 / Validated in CH, DE, ES, FR, GB, IE, IT, NL
14.006011 US PRI
Double-Wall Balloon Catheter for Treatment of Proliferative Tissue
Children:
·     09/293,524
·     09/464,727
·     PCT/US98/12960
08/900,021
5,913,813
 
A-2

 
14.006011 CA
Double Wall Balloon Catheter for Treatment of Proliferative Tissue
2,296,430
2,296,430 (CA)
14.006011 EP
Double Wall Balloon Catheter for Treatment of Proliferative Tissue
DE, FR, and GB Designated
European Patent Application No. 98931470.3
Filed 6/22/98 based on PCT/US87/12960 98 and 08/900,021, filed 7/24/97.
 
14.006011 JP
Double Wall Balloon Catheter for Treatment of Proliferative Tissue
2000-503899
 
Patent Number 3920568
14.006011 JP-DIV
Double Wall Balloon Catheter for Treatment of Proliferative Tissue
Parent: 2000-503899
2005-297129
Patent Number 4002985
14.007011 US PRI
Hazardous Fluid Infuser
Children:
·     PCT/US00/21427
·     09/761,790
09/369,903
6,238,374
14.007011 US CON 1
Radiation Shield for a Syringe
Parent: 6,238,374 (09/369,903)
09/761,790
6,589,158
14.007011 US CON 1
Radiation Shield for a Syringe
Parent: 6,238,374 (09/369,903)
09/761,790
6,589,158
       
14.011011 US PRI
“Brachytherapy Apparatus and Method For Treating A Target Tissue Through An External Surface of The Tissue”
10/704,344
 
Patent Number 7,494,457
 
A-3

 
14.011011 US EP
“Brachytherapy Apparatus and Method For Treating A Target Tissue Through An External Surface of The Tissue”
European Application No. 04810534.0
 
Patent Number 1680188 / Validated in CH, DE, ES, FR, GB, HK, and IE / Waiting for Validation in IT
14.011011 US PCT
“Brachytherapy Apparatus and Method For Treating A Target Tissue Through An External Surface of The Tissue”
PCT/US04/37205
National Phase in AU (2004289269), BR (PI0416261-7), CA (2,544,775), CN (200480039794.7, Now Published 1/24/07 #CN 1901970A), EP (04810534.0, Now Issued 1/9/08 # 1680188), IN (501/MUMNP/06), JP (2006-539712, Now Published 4/26/07 #2007-510513), KR (10-2006-7009300, Now Published 5/11/07 #10-2007-0049597), MX (PA/a/2008/005062, Now Published 10/17/06 #2006/005062), NL (04810534.0)
14.012011 US PRI
Drug Eluting Brachytherapy Methods and Apparatus
10/714,586
7,524,275
14.012011 US PCT
Drug Eluting Brachytherapy Methods and Apparatus
PCT/US04/37560
National Phase in AU (200429107), BR (PI0416502-0), CA (2,545,925), CN (200480040261.0, Now Published 2/21/07 #CN 1917920A), EP (04810703.1, Now Published 6/28/06 #0682225), HK (06111356.9), IN (707/MUMNP/2006), JP (2006-539825, Now Published 5/10/07 #2007-511281), KR (10-06-7009412), MX (PA/a/2006/005352)
 
A-4

 
14.014011 US PRI
Implantable Radiotherapy/Brachytherapy Radiation Detecting Apparatus And Methods
10/704,340
7,354,391
14.014011 US CON
Implantable Radiotherapy/Brachytherapy Radiation Detecting Apparatus And Methods
Parent: 10/704,340
12/046,005
 
14.014011 US PCT
Implantable Radiotherapy/Brachytherapy Radiation Detecting Apparatus And Methods
PCT/US04/36918
National Phase in AU (2004288687), BR (PI0416259-5), CA (2,544,766), CN (200480039793.2, Now Published 1/24/07 #CN 1901969A), EP (04800794.2, Now Published 7/19/06 #1680187), HK (06111353.2), IL (175387, Now Abandoned), IN (503/MUMNP/06), JP (2006-539665, Now Published 4/26/07 #2007-510508), KR (10-2006-7008902, Now Published 1/24/07 #10-2007-0011234), MX (PA/a/2006/005060, Now Allowed)

A-5


APPENDIX B:

Licensed Trademarks:

GLIASITE
Reg. No. 2,315,000 (U.S.)
GLIASITE
Reg. No. 005142245 (CTM)


 
EX-99.1 3 v188853_ex99-1.htm Unassociated Document
 
  
 
FOR IMMEDIATE RELEASE
Contact:
   Sharon Schultz
 
Tel:
   (301) 351-0109
 
email:
   schultzpr@mchsi.com

ISORAY AND HOLOGIC SIGN EXCLUSIVE WORLDWIDE LICENSE FOR

CRUCIAL BRAIN CANCER TREATMENT DEVICE
FDA-Cleared GliaSite® Balloon Catheter Is World's Only Device
to Deliver Liquid Radiation Source Therapy

Richland, WA (June 23, 2010) - - IsoRay, Inc. (Amex: ISR) announced today that it has completed a license agreement with Hologic, Inc. (NASDAQ:HOLX) for exclusive worldwide distribution rights to the GliaSite® radiation therapy system, the world's only FDA-cleared balloon catheter device used in the treatment of brain cancer. The system’s balloon catheter is a landmark technology that allows physicians to treat more patients than ever before with brachytherapy or internal radiation and provides important benefits over other radiation treatment options.

Brain cancer presents unique treatment challenges. Brain tumors are very often difficult to remove completely because of the need to avoid damaging the brain.  Further, tumors tend to spread to healthy parts of the brain. Typically, surgeons remove as much as they can of the tumor and then treat the areas surrounding where the tumor was removed with radiation therapy. They sometimes use chemotherapy as well.  However, most cancerous brain tumors reoccur shortly following removal, and the cancer tends to return near the site of the original tumor. Brain cancer is one of the fastest growing cancers and recurrence often proves fatal.

The GliaSite system offers a number of advantages in brain cancer treatment.  It places a specified high dose of a liquid radiation source in the areas most likely to contain cancer after brain tumor removal and is less likely to damage healthy brain tissue.  It helps eliminate the ability for the tumor to reoccur, which in turn impacts patient longevity.

In a related major development, IsoRay is moving forward with the regulatory approval process for its new liquid form of Cesium-131, an exciting advance in brachytherapy for the treatment of brain cancer, that would be delivered using the GliaSite radiation therapy system.

IsoRay CEO Dwight Babcock said physicians have voiced strong support for the GliaSite system and liquid Cesium-131 combination because they recognize the benefits afforded their patients. "In America alone, more than 200,000 men, women, and children are diagnosed with brain cancers every year. The GliaSite therapy system and its use to deliver a liquid radiation source is a versatile, effective treatment for numerous brain cancers," he said.
 
 
 

 
 
Cesium-131 brachytherapy is a patented internal radiation therapy that has several advantages over older radioactive isotopes including faster delivery of a radiation dose that allows less time and opportunity for the cancer cells to repopulate and has a soft energy that minimizes radiation exposure for the operating room and support staff as well as the patient's family members.

Babcock said this is another step forward in IsoRay's efforts to advance cancer treatment.  "Progress spells hope for patients and the physicians who help them. The GliaSite system represents further achievement as we work toward our goal of expanding brachytherapy solutions throughout the entire body and improving outcomes for cancer patients," said Babcock.

Previously, approximately 500 GliaSite cases were performed annually at some 40 hospitals worldwide.   GliaSite therapy has established reimbursement for both in-patient and out-patient settings.

About IsoRay
IsoRay, Inc., through its subsidiary, IsoRay Medical, Inc., is the sole producer of Cesium-131 brachytherapy seeds, which are expanding brachytherapy options throughout the body.  Learn more about this innovative Richland, Washington company and explore the many benefits and uses of Cesium-131 by visiting www.isoray.com.

GliaSite is a trademark or registered trademark of Hologic and/or Hologic subsidiaries in the Unites States and/or other countries.

Safe Harbor Statement
Statements in this news release about IsoRay's future expectations, including: the advantages of our Proxcelan Cesium-131 seed, the advantages of the Gliasite delivery system, whether a liquid form of Cesium-131 will be developed that receives regulatory approval and can be used successfully with the Gliasite delivery system, whether IsoRay will be able to expand its base beyond prostate cancer, whether IsoRay's Cesium-131 seed will be used to treat additional cancers and malignant disease, whether the use of Cesium-131 to treat brain or other cancers will be successful in the initial and any future implants, and all other statements in this release, other than historical facts, are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995 ("PSLRA"). This statement is included for the express purpose of availing IsoRay, Inc. of the protections of the safe harbor provisions of the PSLRA.  It is important to note that actual results and ultimate corporate actions could differ materially from those in such forward-looking statements based on such factors as physician acceptance, training and use of our products, our ability to successfully manufacture, market and sell our products, our ability to manufacture our products in sufficient quantities to meet demand within required delivery time periods while meeting our quality control standards, our ability to enforce our intellectual property rights, whether additional studies are released and support the conclusions of early clinical studies, whether initial implants of Cesium-131 to treat brain or other cancers result in favorable patient outcomes, whether resources are available as needed to develop a liquid form of Cesium-131 and whether such liquid form receives and maintains all required regulatory approvals, whether any liquid form of Cesium-131 is able to be used successfully with the Gliasite delivery system, patient results achieved when Cesium-131 is used for the treatment of cancers and malignant diseases beyond prostate cancer whether with the Gliasite delivery system or in another delivery system, successful completion of future research and development activities, and other risks detailed from time to time in IsoRay's reports filed with the SEC.

 
 

 
 
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-----END PRIVACY-ENHANCED MESSAGE-----