Genocea Provides Third Quarter 2020 Corporate Update

Initiated GEN-011 Phase1/2a clinical trial

Presented positive follow-up GEN-009 Part B data at ESMO Virtual Congress 2020 demonstrating potential added benefit to PD-1 inhibitor therapy

Closed financing with net proceeds of $74.5 million

Upcoming presentations at SITC 2020 Virtual Conference on GEN-009, Inhibigens


and GEN-011

Conference call today at 8:30 a.m. EDT

CAMBRIDGE, Mass., Oct. 29, 2020 (GLOBE NEWSWIRE) —

Genocea Biosciences, Inc


(NASDAQ: GNCA), a biopharmaceutical company developing next-generation neoantigen immunotherapies, today reported its operating and financial results for the third quarter ended September 30, 2020.

GEN-011 Phase 1/2a clinical trial initiation

Genocea recently announced the U.S. Food and Drug Administration (FDA) accepted the company’s Investigational New Drug (IND) Application for GEN-011, an adoptive neoantigen T cell therapy designed to improve upon the limitations of TIL and TCR therapies. The company initiated a Phase 1/2a clinical study of GEN-011 in patients who have failed standard-of-care checkpoint inhibitor therapy to evaluate safety, T cell proliferation and persistence as well as clinical activity. Genocea plans to enroll up to 24 patients across several tumor types in the trial.

Scientific and clinical presentations: ESMO Congress, upcoming SITC meeting and conference call

Genocea presented clinical response and immunogenicity data on the first five patients from Part B of the ongoing GEN-009 Phase 1/2a trial at the European Society for Medical Oncology (ESMO) Virtual Congress 2020. The incremental follow-up findings demonstrated tumor reductions or stable outcomes for all five patients, suggesting GEN-009 vaccination could be used in conjunction with CPI-based therapies to augment their effects. In addition, 100% of patients demonstrated immune responses to ATLAS™-identified neoantigens.

Genocea will report additional clinical and immunogenicity data from the remaining GEN-009 Part B patients during the 2020 virtual Society for Immunotherapy of Cancer (SITC) annual meeting from November 9-14. The company will also provide a detailed introduction to GEN-011 and will share new insights on the utility of ATLAS-identified Inhibigens to inform future immunotherapy development.

Genocea will host a conference call on Monday, November 9 at 8:30 a.m. EST to discuss the new GEN-009 clinical and immunogenicity data reported at SITC.

Private placement

In July, Genocea completed a private placement with $74.5 million in net proceeds. The proceeds will be used to fund continued development of GEN-009, GEN-011 and ATLAS.

“In the third quarter, our team achieved important clinical, scientific and financial progress. We provided what we believe to be differentiated immunogenicity and efficacy data from an initial look at our GEN-009 Part B clinical trial and secured critical fresh capital”, said Chip Clark, president and chief executive officer Genocea. “Using these proceeds to advance GEN-011 into the clinic and to further our investigation into ATLAS and its applications represents an exciting opportunity.”

Third Quarter 2020 Financial Results

  • Cash position

    : As of September 30, 2020, cash and cash equivalents were $87.6 million versus $40.1 million as of December 31, 2019.

  • Research and Development (R&D) expenses

    : R&D expenses were $7.5 million for the quarter ended September 30, 2020, compared to $6.8 million for the same period in 2019.

  • General and Administrative (G&A) expenses

    : G&A expenses were $3.6 million for the quarter ended September 30, 2020, compared to $2.8 million for the same period in 2019.

  • Net loss

    : Net loss was $4.6 million for the quarter ended September 30, 2020, compared to $7.5 million for the same period in 2019.


Genocea expects that its existing cash and cash equivalents are sufficient to support its operations to mid-2022.

Conference Call

Genocea will host a conference call and webcast today at 8:30 a.m. EDT. Interested participants may access the conference call by dialing (844) 826-0619 (domestic) or (315) 625-6883 (international) and referring to conference ID number 5951388. To join the live webcast, please visit the presentation page of the investor relations section of the Genocea website at

. A webcast replay of the conference call will be available on the Genocea website beginning approximately two hours after the event and will be archived for 90 days.

About Genocea Biosciences, Inc.

Genocea’s mission is to conquer cancer by developing personalized cancer immunotherapies in multiple tumor types. Our unique ATLAS™ platform comprehensively profiles each patient’s T cell responses to potential targets, or antigens, on the tumor. ATLAS enables us to optimize the neoantigens for inclusion in our immunotherapies and exclude inhibitory antigens that can exert an immunosuppressive effect. We are advancing two ATLAS-enabled programs: GEN-009, our neoantigen vaccine for which we are conducting a Phase 1/2a clinical trial and GEN-011, our neoantigen-specific cell therapy using T cells derived from peripheral blood for which we are commencing a Phase 1/2a clinical trial. To learn more, please visit

Forward-Looking Statements

This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act. Such forward-looking statements are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied in such statements. Genocea cautions that these forward-looking statements are subject to numerous assumptions, risks and uncertainties that change over time. Applicable risks and uncertainties include those identified under the heading “Risk Factors” included in Genocea’s Annual Report on Form 10-K for the year ended December 31, 2019 and any subsequent SEC filings. These forward-looking statements speak only as of the date of this press release and Genocea assumes no duty to update forward-looking statements, except as may be required by law.

Investor Contact:

Dan Ferry


[email protected]

(Tables to follow)



(In thousands)

September 30, 2020 December 31, 2019
Cash and cash equivalents $ 87,625 $ 40,127
Right of use assets 10,737 6,306
Other assets 7,836 6,178
Total assets $ 106,198 $ 52,611
Accounts payable and accrued expenses $ 6,351 $ 5,164
Deferred revenue 1,641
Debt, current and long-term 13,743 13,407
Warrant liabilities 53,237 2,486
Lease liabilities 11,021 6,512
Total liabilities 85,993 27,569
Stockholders’ equity 20,205 25,042
Total liabilities and stockholders’ equity $ 106,198 $ 52,611



(In thousands, except per share data)

Three Months Ended

September 30,
Nine Months Ended

September 30,
2020 2019 2020 2019
License revenue $ 453 $ $ 1,359 $
Operating expenses:
Research and development 7,548 6,826 26,123 20,135
General and administrative 3,644 2,758 10,511 8,992
Total operating expenses 11,192 9,584 36,634 29,127
Loss from operations (10,739 ) (9,584 ) (35,275 ) (29,127 )
Other income (expense) 6,184 2,052 6,546 (467 )
Net loss $ (4,555 ) $ (7,532 ) $ (28,729 ) $ (29,594 )
Net loss per share:
Basic $ (0.08 ) $ (0.28 ) $ (0.76 ) $ (1.62 )
Diluted $ (0.26 ) $ (0.28 ) $ (1.01 ) $ (1.62 )
Weighted-average number of shares used in computing net loss per share:
Basic 55,492 26,681 37,657 18,297
Diluted 61,130 26,681 39,550 18,297

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