0001193125-22-218611.txt : 20220811 0001193125-22-218611.hdr.sgml : 20220811 20220811163810 ACCESSION NUMBER: 0001193125-22-218611 CONFORMED SUBMISSION TYPE: 8-K PUBLIC DOCUMENT COUNT: 14 CONFORMED PERIOD OF REPORT: 20220811 ITEM INFORMATION: Results of Operations and Financial Condition ITEM INFORMATION: Financial Statements and Exhibits FILED AS OF DATE: 20220811 DATE AS OF CHANGE: 20220811 FILER: COMPANY DATA: COMPANY CONFORMED NAME: IO Biotech, Inc. CENTRAL INDEX KEY: 0001865494 STANDARD INDUSTRIAL CLASSIFICATION: PHARMACEUTICAL PREPARATIONS [2834] IRS NUMBER: 870909276 STATE OF INCORPORATION: DE FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 8-K SEC ACT: 1934 Act SEC FILE NUMBER: 001-41008 FILM NUMBER: 221156483 BUSINESS ADDRESS: STREET 1: OLE MAALOES VEH 3 CITY: COPENHAGEN STATE: G7 ZIP: 2200 BUSINESS PHONE: 4570702980 MAIL ADDRESS: STREET 1: OLE MAALOES VEH 3 CITY: COPENHAGEN STATE: G7 ZIP: 2200 8-K 1 d359264d8k.htm 8-K 8-K
false 0001865494 0001865494 2022-08-11 2022-08-11

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 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): August 11, 2022

 

 

IO BIOTECH, INC.

(Exact name of Registrant as Specified in its Charter)

 

 

 

Delaware   001-41008   87-0909276

(State or other jurisdiction

of incorporation)

 

(Commission

File Number)

 

(IRS Employer

Identification No.)

Ole Maaløes Vej 3

DK-2200 Copenhagen N

Denmark

(Address of principal executive offices) (Zip Code)

Registrant’s telephone number, including area code: +45 7070 2980

N/A

(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 (see General Instruction A.2. below):

 

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 (17 CFR 240.14a-12)

 

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

 

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

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class

 

Trading
Symbol(s)

 

Name of each exchange

on which registered

Common Stock, par value $0.001 per share   IOBT   The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company  

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.  

 

 

 


Item 2.02

Results of Operations and Financial Condition

On August 11, 2022, IO Biotech, Inc. (the “Company”) issued a press release announcing its financial results for the quarter ended June 30, 2022 and an update on the Company’s operations for the same period. The Company is furnishing a copy of the press release, which is attached hereto as Exhibit 99.1.

In accordance with General Instruction B.2 of Form 8-K, the information included in this Item 2.02, including Exhibit 99.1 hereto, shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any filing made by the Company under the Exchange Act or Securities Act of 1933, as amended, except as shall be expressly set forth by specific reference in such a filing.

 

Item 9.01

Financial Statements and Exhibits.

(d) Exhibits

 

Exhibit

No.

   Description
99.1    Press Release of the Company, dated August 11, 2022
104    Cover Page Interactive Data File (embedded within the Inline XBRL document)


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.

 

    IO BIOTECH, INC.
Date: August 11, 2022     By:  

/s/ Mai-Britt Zocca

    Name:   Mai-Britt Zocca, Ph.D.
    Title:   Chief Executive Officer
EX-99.1 2 d359264dex991.htm EX-99.1 EX-99.1

Exhibit 99.1

 

LOGO

IO Biotech Announces Second Quarter Results for 2022

 

   

Announced initiation and dosing of first patient in global Phase 3 combination trial of IO102-IO103 and KEYTRUDA® (pembrolizumab) as first-line treatment in advanced melanoma

 

   

Announced initiation and dosing of first patient in Phase 2 Trial of IO102-IO103 in combination with KEYTRUDA® (pembrolizumab) as first line treatment in multi-cohort basket trial

 

   

Two presentations at ASCO highlighted current clinical trials with IO102-IO103 in combination with pembrolizumab and updated data cut from Phase 1/2 study of IO102-IO103 in combination with nivolumab showing high response rates in metastatic melanoma presented at AACR

 

   

Strong balance sheet with $170.1 million cash runway to support multiple expected data readouts into mid-2024

New York, New York – August 11, 2022: IO Biotech (Nasdaq: IOBT), a clinical-stage biopharmaceutical company developing novel, immune-modulating cancer therapies based on its T-win® technology platform, announced today financial results for the quarter ending June 30, 2022.

“We continue to advance our promising pipeline of novel cancer immunotherapies following clinical trial milestones achieved in the first half of the year,” said Mai-Britt Zocca, Ph.D., President and Chief Executive Officer of IO Biotech. “During the quarter we were pleased to announce the initiation and dosing of first patients our Phase 3 global combination trial of IOB102-103 with pembrolizumab as a potential first line treatment in advanced melanoma. We look forward to enrolling patients across the U.S., Australia and Europe. We will provide an update on the anticipated timing of the interim data once we have sufficient information. During the quarter, we also announced the initiation and dosing of the first patient in our Phase 2 basket trial of IO102-IO103 in combination with pembrolizumab. We expect to receive preliminary data in one indication in the second half of 2022, and additional data in 2023.

“In June, we shared two poster presentations highlighting clinical trials in progress with IO102-IO103 in combination with pembrolizumab in metastatic solid tumors and in untreated, unresectable or metastatic melanoma at the ASCO 2022 Annual Meeting. We are excited to build on the promising clinical activity seen from our previous Phase 1/2 clinical trial evaluating IO102-IO103 in metastatic melanoma as we believe that our T-win® platform—and its novel approach to activate naturally occurring T cells to target immunosuppressive mechanisms—has the potential to benefit patients in need of more treatment options. With a solid balance sheet and substantial cash runway to carry us through multiple expected data readouts into mid-2024, we look forward to sharing further progress in the coming months.”

 

IO Biotech ApS

Ole Maaløes Vej 3

2200 Copenhagen N, Denmark

www.iobiotech.com

   Page 1 of 6


LOGO

 

Highlights for Second Quarter 2022 and Recent Weeks

 

   

Announced initiation and dosing of the first patient in the Phase 3 IOB-013/KN-D18 trial of IO102-IO103 and KEYTRUDA® (pembrolizumab) as first-line treatment in advanced melanoma (NCT05155254);

 

   

Announced initiation and dosing of the first patient in the Phase 2 IOB-022/KN-D38 basket trial in solid tumors (NCT05077709) in April 2022;

 

   

Announced the presentation of two posters highlighting clinical trials in progress with IO102-IO103 as an investigational agent in combination with pembrolizumab in metastatic solid tumors and in untreated, unresectable or metastatic melanoma at the 2022 American Society of Clinical Oncology (ASCO) Annual Meeting.

 

   

Hosted Part 1 of Key Opinion Leader Webinar Series: A New Way to Kill Tumors–IO102-IO103 Phase 3 Trial in Combination with Anti-PD-1 in Advanced Melanoma

 

   

New data from MM1636 Phase 1/2 clinical trial presented at 2022 American Association for Cancer Research (AACR) Annual Meeting

 

   

Three-year overall survival probability of 73%

 

   

Subgroup analyses including patients with poor prognosis

Second Quarter Financial Results

 

   

Net loss for the three months ended June 30, 2022 was $18.5 million, compared to $38.4 million for the quarter ended June 30, 2021.

 

   

Research and development expenses were $12.2 million for the three months ended June 30, 2022, compared to $6.7 million for the three months ended June 30, 2021. The increase of $5.5 million was primarily related to an increase in preclinical studies and clinical trial-related activities for our IO102-IO103 product candidate, including the initiation of our Phase 3 clinical trial, of $2.6 million, an increase in costs for chemistry, manufacturing and control, activities of $0.5 million, and an increase in personnel costs of $2.1 million primarily related to an increase in headcount and related recruiting costs.

 

   

General and administrative expenses were $5.9 million for the three months ended June 30, 2022, compared to $2.2 million for the three months ended June 30, 2021. The increase of $3.7 million was primarily related to an increase in personnel costs of $1.5 million primarily related to an increase in headcount and related recruiting costs and an increase in consultants and other costs of $2.7 million, partially offset by a decrease in professional services of $0.5 million related primarily to corporate legal fees and audit and tax fees.

 

   

Other expense was a net expense of $0.2 million for the three months ended June 30, 2022 compared to a net expense of $29.4 million for the three months ended June 30, 2021. The increase of $29.2 million was mainly due to fair-value adjustments on preferred stock tranche obligations were losses of $29.4 million for the three months ended June 30, 2021.

 

IO Biotech ApS

Ole Maaløes Vej 3

2200 Copenhagen N, Denmark

www.iobiotech.com

   Page 2 of 6


LOGO

 

   

Cash and cash equivalents at June 30, 2022 were $170.1 million, compared to $211.5 million at December 31, 2021. Cash on hand is expected to support operations through anticipated data readouts into mid-2024.

About the IOB-013/KN-D18 Clinical Trial

IOB-013/KN-D18 (Clinical Trials.gov: NCT05155254) is an open label, randomized Phase 3 clinical trial being conducted in collaboration with Merck of IO102-IO103 in combination with pembrolizumab versus pembrolizumab alone in patients with previously untreated, unresectable or metastatic (advanced) melanoma. Target enrollment will be 300 patients from centers spread across Europe, Australia, and the United States. Biomarker analyses will also be conducted. IO Biotech will sponsor the Phase 3 trial and Merck will supply pembrolizumab. IO Biotech maintains global commercial rights to IO102-IO103.

About IOB-022/KN-D38

IOB-022/KN-D38 is a non-comparative, open label trial to investigate the safety and efficacy of IO102-IO103 in combination with pembrolizumab in each of the following first-line indications: NSCLC, SCCHN, and mUBC. The clinical trial will be sponsored by IO Biotech and conducted in collaboration with Merck. IO Biotech maintains global commercial rights to IO102-IO103.

About IO102-IO103

IO102-IO103 is an investigational cancer immunotherapy designed to target the

immunosuppressive mechanisms mediated by the key immunosuppressive proteins indoleamine 2,3-dioxygenase (IDO) and PD-L1.

About IO Biotech

IO Biotech is a clinical-stage biopharmaceutical company developing novel, immune-modulating cancer therapies based on its T-win® technology platform. The T-win® platform is a novel approach to cancer immunotherapy designed to activate naturally occurring T cells to target immunosuppressive mechanisms. IO Biotech is advancing in clinical studies its lead immuno-oncology candidate, IO102-IO103, targeting IDO and PD-L1, and through clinical and preclinical development its other pipeline candidates. IO Biotech is headquartered in Copenhagen, Denmark and has additional offices within the United States (New York, New York and Rockville, Maryland) and United Kingdom (Monmouthshire).

For further information, please visit www.iobiotech.com

 

IO Biotech ApS

Ole Maaløes Vej 3

2200 Copenhagen N, Denmark

www.iobiotech.com

   Page 3 of 6


LOGO

 

Forward-Looking Statement

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements, including regarding future clinical trials and results, are based on IO Biotech’s current assumptions and expectations of future events and trends, which affect or may affect its business, strategy, operations or financial performance, and actual results and other events may differ materially from those expressed or implied in such statements due to numerous risks and uncertainties. Forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified. Because forward-looking statements are inherently subject to risks and uncertainties, you should not rely on these forward-looking statements as predictions of future events. These forward-looking statements speak only as of the date hereof and should not be unduly relied upon. Except to the extent required by law, IO Biotech undertakes no obligation to update these statements, whether as a result of any new information, future developments or otherwise.

Company Contact:

Mai-Britt Zocca, Ph.D.

President and CEO

IO Biotech, Inc.

mz@iobiotech.com

Investor Contact:

Corey Davis, Ph.D.

LifeSci Advisors

212-915-2577

cdavis@lifesciadvisors.com

Media Contact:

Raena Mina, Ph.D.

LifeSci Communications

646-606-1438

rmina@lifescicomms.com

KEYTRUDA® is a registered trademark of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA.

—tables to follow—

 

IO Biotech ApS

Ole Maaløes Vej 3

2200 Copenhagen N, Denmark

www.iobiotech.com

   Page 4 of 6


LOGO

 

IO BIOTECH, INC.

Condensed Consolidated Statements of Operations and Comprehensive Loss

(In thousands, except share and per share amounts)

(unaudited)

 

     For the Three Months
Ended June 30,
    Six Months Ended
June 30,
 
     2022     2021     2022     2021  

Operating expenses

        

Research and development

   $ 12,226     $ 6,735     $ 22,531     $ 9,583  

General and administrative

     5,935       2,248       12,639       3,213  
  

 

 

   

 

 

   

 

 

   

 

 

 

Total operating expenses

     18,161       8,983       35,170       12,796  
  

 

 

   

 

 

   

 

 

   

 

 

 

Loss from operations

     (18,161     (8,983     (35,170     (12,796
  

 

 

   

 

 

   

 

 

   

 

 

 

Other income (expense)

        

Currency exchange gain (loss), net

     (286     155       (305     292  

Interest income

     158       —         173       —    

Interest expense

     (102     (71     (226     (143

Fair value adjustments on preference shares tranche obligations

     —         (29,460     —         (29,460
  

 

 

   

 

 

   

 

 

   

 

 

 

Total other income (expense), net

     (230     (29,376     (358     (29,311
  

 

 

   

 

 

   

 

 

   

 

 

 

Loss before income tax expense

     (18,391     (38,359     (35,528     (42,107

Income tax expense

     104       —         171       —    
  

 

 

   

 

 

   

 

 

   

 

 

 

Net loss

     (18,495     (38,359     (35,699     (42,107

Cumulative dividends on class B and C preference shares

     —         (2,094     —         (3,933
  

 

 

   

 

 

   

 

 

   

 

 

 

Net loss attributable to common shareholders

     (18,495     (40,453     (35,699     (46,040
  

 

 

   

 

 

   

 

 

   

 

 

 

Net loss per common share, basic and diluted

   $ (0.64   $ (228.29   $ (1.24   $ (259.82
  

 

 

   

 

 

   

 

 

   

 

 

 

Weighted-average number of shares used in computing net loss per common share, basic and diluted

     28,815,267       177,200       28,815,267       177,200  
  

 

 

   

 

 

   

 

 

   

 

 

 

Other comprehensive loss

        

Net loss

     (18,495     (38,359     (35,699     (42,107

Foreign currency translation

     (4,379     1,190       (7,026     (576
  

 

 

   

 

 

   

 

 

   

 

 

 

Total comprehensive loss

     (22,874     (37,169     (42,725     (42,683
  

 

 

   

 

 

   

 

 

   

 

 

 

 

IO Biotech ApS

Ole Maaløes Vej 3

2200 Copenhagen N, Denmark

www.iobiotech.com

   Page 5 of 6


LOGO

 

IO BIOTECH, INC.

Condensed Consolidated Balance Sheets

(In thousands, except share and per share amounts)

(unaudited)

 

     June 30,
2022
    December 31,
2021
 

Assets

    

Current assets

    

Cash and cash equivalents

   $ 170,122     $ 211,531  

Prepaid expenses and other current assets

     8,839       10,207  
  

 

 

   

 

 

 

Total current assets

     178,961       221,738  

Restricted cash

     268       268  

Property and equipment, net

     358       155  

Right of use lease asset

     2,148       —    

Noncurrent assets

     910       127  
  

 

 

   

 

 

 

Total assets

   $ 182,645     $ 222,288  
  

 

 

   

 

 

 

Liabilities, convertible preference shares and stockholders’ equity

    

Current liabilities

    

Accounts payable

   $ 4,541     $ 3,928  

Lease liability - current

     419       —    

Accrued expenses and other current liabilities

     3,587       6,377  
  

 

 

   

 

 

 

Total current liabilities

     8,547       10,305  

Lease liability - noncurrent

     1,921       —    

Other long-term liabilities

     —         59  
  

 

 

   

 

 

 

Total liabilities

     10,468       10,364  
  

 

 

   

 

 

 

Convertible preference shares

    

Stockholders’ equity

    

Preferred stock, par value of $0.001 per share; 5,000,000 shares authorized, no shares issued and outstanding as of June 30, 2022 and December 31, 2021

     —         —    

Common stock, par value of $0.001 per share; 300,000,000 shares authorized, 28,815,267 shares issued and outstanding as of June 30, 2022 and December 31, 2021

     29       29  

Additional paid-in capital

     322,643       319,665  

Accumulated deficit

     (141,980     (106,281

Accumulated other comprehensive loss

     (8,515     (1,489
  

 

 

   

 

 

 

Total stockholders’ equity

     172,177       211,924  
  

 

 

   

 

 

 

Total liabilities, convertible preference shares and stockholders’ equity

   $ 182,645     $ 222,288  
  

 

 

   

 

 

 

 

IO Biotech ApS

Ole Maaløes Vej 3

2200 Copenhagen N, Denmark

www.iobiotech.com

   Page 6 of 6
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Document and Entity Information
Aug. 11, 2022
Cover [Abstract]  
Amendment Flag false
Entity Central Index Key 0001865494
Document Type 8-K
Document Period End Date Aug. 11, 2022
Entity Registrant Name IO BIOTECH, INC.
Entity Incorporation State Country Code DE
Entity File Number 001-41008
Entity Tax Identification Number 87-0909276
Entity Address, Address Line One Ole Maaløes Vej 3
Entity Address, Postal Zip Code DK-2200
Entity Address, City or Town Copenhagen N
Entity Address, Country DK
City Area Code +45
Local Phone Number 7070 2980
Written Communications false
Soliciting Material false
Pre Commencement Tender Offer false
Pre Commencement Issuer Tender Offer false
Security 12b Title Common Stock, par value $0.001 per share
Trading Symbol IOBT
Security Exchange Name NASDAQ
Entity Emerging Growth Company true
Entity Ex Transition Period false
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