Gritstone Reports Third Quarter 2021 Financial Results and Business Update
- Phase 1 data from Gritstone-sponsored CORAL study (SARS-CoV-2 second generation vaccine utilizing self-amplifying mRNA boost) expected in early Q1 2022; CORAL is a multi-trial vaccine program which seeks to drive broad and durable immune responses to SARS-CoV-2 variants
- Data presented during ESMO 2021 show robust clinical and molecular responses and favorable safety profile across difficult to treat solid tumors with GRANITE (individualized neoantigen program) and SLATE (off-the-shelf shared neoantigen program)
- Cash, cash equivalents, marketable securities and restricted cash of
$216.4 million as ofSeptember 30, 2021
“We are pleased with our strengthened cash position and the significant clinical progress achieved during this third quarter,” said
Corporate Highlights
- Entered into a funding agreement of up to
$20.6 million with theCoalition for Epidemic Preparedness Innovations (CEPI) to advance the clinical development of Gritstone’s CORAL second generation mRNA COVID-19 vaccine program, including a clinical trial inSouth Africa and manufacturing optimization (CEPI Press Release,August 2021 ) - Received gross proceeds of
$55.0 million from a private investment in public equity (PIPE) financing led byFrazier Life Sciences Public Fund , with additional participation fromRedmile Group and Gilead Sciences (PIPE Press Release,September 2021 )
Clinical Highlights and Updates
Tumor-Specific Neoantigen (TSNA) Oncology Programs
GRANITE – Individualized, TSNA-directed immunotherapy using an adenoviral priming vector and self-amplifying mRNA boost vector
- Updated Phase 1/2 results evaluating the safety, immunogenicity and clinical activity of GRANITE individualized neoantigen immunotherapy in combination with PD-1 checkpoint inhibitor nivolumab and subcutaneous anti-CTLA-4 antibody ipilimumab in advanced solid tumors presented at ESMO 2021 (GRANITE Press Release,
September 2021 ) - GRANITE immunotherapy demonstrated a 44% molecular response rate (4/9) as measured by >50% reduction in circulating tumor DNA (ctDNA) with associated median overall survival >17 months in patients with end-stage microsatellite-stable colorectal cancer (MSS-CRC) for whom median overall survival is typically 6-7 months (as observed in the 5/9 patients without molecular response)
- A Phase 2/3 randomized, controlled trial of maintenance GRANITE immunotherapy in newly diagnosed metastatic, MSS-CRC patients is expected to initiate in the first quarter of 2022
- This Phase 2/3 trial has registrational intent and has been discussed with the FDA
- A Phase 2 randomized trial of adjuvant GRANITE immunotherapy in MSS-CRC patients with stage II/III disease who are ctDNA+ after definitive surgery is expected to initiate in the second quarter of 2022
SLATE – “Off-the-shelf” shared neoantigen-directed immunotherapy using an adenoviral priming vector and self-amplifying mRNA boost vector
- Presented Phase 1/2 data demonstrating SLATE v1 + nivolumab + ipilimumab in 26 patients with metastatic solid tumors
- Observed multiple molecular responses and an unconfirmed RECIST radiologic response were observed in patients with metastatic NSCLC, all of whom had progressed on prior (chemo)immunotherapy (SLATE Press Release,
September 2021 ) - SLATE v2, a mutant KRAS-focused version optimized for increased immune response, is currently being evaluated in a Phase 2 trial in patients with NSCLC and MSS-CRC. Initial clinical data are anticipated by mid-2022.
Infectious Disease Programs
CORAL – second-generation SARS-CoV-2 vaccine program delivering both spike and highly conserved non-spike T cell epitopes within either a self-amplifying mRNA vector or an optimized chimpanzee adenoviral vector (ChAdV). This approach offers potential for more durable clinical protection and broader immunity against SARS-CoV-2 variants than 1st generation products by inducing potent CD8+ T cells in addition to neutralizing antibody responses
- Dosed first volunteer in a company-sponsored Phase 1 trial evaluating GRT-R910, a self-amplifying mRNA (SAM) second generation SARS-CoV-2 vaccine designed to boost and expand the immunogenicity of first-generation COVID-19 vaccines in subjects 60 years of age or older. (GRT-R910 Press Release,
September 2021 )- Initial Phase 1 data from this study are expected early in the first quarter 2022
- Our collaboration with the
National Institute of Allergy and Infectious Disease (NIAID) to evaluate the safety, tolerability and immunogenicity of investigational ChAdV and SAM SARS-CoV-2 vaccines continues:- Non-human primate viral challenge data are expected in
November 2021 - Preliminary results from a Phase 1 trial are now expected in the first half of 2022 due to protocol amendments necessitated by the changing landscape of vaccine use in
the United States
- Non-human primate viral challenge data are expected in
Third Quarter 2021 Financial Results
- Cash, cash equivalents. marketable securities and restricted cash were
$216.4 million as ofSeptember 30, 2021 compared to$172.1 million as ofDecember 31, 2020 . - Research and development expenses were
$24.4 million for the three months endedSeptember 30, 2021 , compared to$22.1 million for the three months endedSeptember 30, 2020 . The increase was primarily due to increases of$1.7 million in personnel-related expenses and$2.4 million in outside services, offset by$1.8 million decreases in laboratory supplies. - General and administrative expenses were
$6.4 million for the three months endedSeptember 30, 2021 , compared to$5.0 million for the three months endedSeptember 30, 2020 . The increase was primarily attributable to increases in personnel-related expenses and outside services. - Collaboration revenue was
$2.4 million for the three months endedSeptember 30, 2021 , compared to$0.8 million for the three months endedSeptember 30, 2020 . The increase was due to the collaboration revenue associated with the collaboration agreement with Gilead fromJanuary 2021 .
About Gritstone
Gritstone Forward-Looking Statements
This press release contains forward-looking statements, including, but not limited to, statements related to Gritstone bio, Inc.’s (“Gritstone”, “we” or “our”) preclinical and clinical product candidates, including GRANITE, SLATE, CORAL, and HIV programs; the advancements in our ongoing clinical trials; the timing of data announcements related to ongoing clinical trials and the initiation of future clinical trials. Such forward-looking statements involve substantial risks and uncertainties that could cause Gritstone’s research and clinical development programs, future results, performance or achievements to differ significantly from those expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, the uncertainties inherent in the drug development process, including Gritstone’s programs’ early stage of development, the process of designing and conducting preclinical and clinical trials, the regulatory approval processes, the timing of regulatory filings, the challenges associated with manufacturing drug products, Gritstone’s ability to successfully establish, protect and defend its intellectual property and other matters that could affect the sufficiency of existing cash to fund operations. Forward-looking statements generally contain words such as "believes," "expects," "may," "will," "should," "seeks," "approximately," "intends," "plans," "estimates," "anticipates," and other expressions that are predictions of or indicate future events and trends and that do not relate to historical matters. Gritstone undertakes no obligation to update or revise any forward-looking statements. For a further description of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to the business of the company in general, see Gritstone’s most recent Quarterly Report on Form 10-Q filed on
Condensed Consolidated Statements of Operations | ||||||||||||||||
(Unaudited) | ||||||||||||||||
(In thousands, except share and per share amounts) | ||||||||||||||||
Three Months Ended | Nine Months Ended | |||||||||||||||
2021 | 2020 | 2021 | 2020 | |||||||||||||
Collaboration revenue | $ | 2,401 | $ | 795 | $ | 44,937 | $ | 2,544 | ||||||||
Grant revenue | 213 | 144 | 213 | 144 | ||||||||||||
Total revenues | 2,614 | 939 | 45,150 | 2,688 | ||||||||||||
Operating expenses: | ||||||||||||||||
Research and development | 24,396 | 22,050 | 71,324 | 65,807 | ||||||||||||
General and administrative | 6,373 | 5,031 | 19,251 | 15,751 | ||||||||||||
Total operating expenses | 30,769 | 27,081 | 90,575 | 81,558 | ||||||||||||
Loss from operations | (28,155 | ) | (26,142 | ) | (45,425 | ) | (78,870 | ) | ||||||||
Interest income, net | 37 | 69 | 112 | 723 | ||||||||||||
Net loss | $ | (28,118 | ) | $ | (26,073 | ) | $ | (45,313 | ) | $ | (78,147 | ) | ||||
Net loss per common share, basic and diluted | $ | (0.36 | ) | $ | (0.69 | ) | $ | (0.59 | ) | $ | (2.10 | ) | ||||
Shares used to compute for net loss per common share, basic and diluted |
77,775,479 | 37,750,145 | 76,837,503 | 37,268,318 | ||||||||||||
Condensed Consolidated Balance Sheets | ||||||||||||||||
(Unaudited) | ||||||||||||||||
(In thousands) | ||||||||||||||||
2021 |
2020 |
|||||||||||||||
Assets | ||||||||||||||||
Current assets: | ||||||||||||||||
Cash and cash equivalents | $ | 131,423 | $ | 170,056 | ||||||||||||
Marketable securities | 68,255 | 1,002 | ||||||||||||||
Restricted cash | 10,995 | - | ||||||||||||||
Prepaid expenses and other current assets | 7,728 | 4,332 | ||||||||||||||
Total current assets | 218,401 | 175,390 | ||||||||||||||
Restricted cash | 5,687 | 992 | ||||||||||||||
Property and equipment, net | 21,337 | 22,105 | ||||||||||||||
Operating lease right-of-use assets | 23,793 | 21,344 | ||||||||||||||
Deposits and other long-term assets | 2,064 | 1,736 | ||||||||||||||
Total assets | $ | 271,282 | $ | 221,567 | ||||||||||||
Liabilities and stockholders' equity | ||||||||||||||||
Current liabilities: | ||||||||||||||||
Accounts payable | $ | 3,393 | $ | 9,578 | ||||||||||||
Accrued compensation | 6,115 | 6,331 | ||||||||||||||
Accrued liabilities | 3,022 | 677 | ||||||||||||||
Accrued research and development | 2,540 | 1,053 | ||||||||||||||
Lease liabilities, current portion | 7,458 | 5,874 | ||||||||||||||
Deferred revenue, current portion | 13,786 | 3,475 | ||||||||||||||
Total current liabilities | 36,314 | 26,988 | ||||||||||||||
Other non-current liabilities | 395 | 395 | ||||||||||||||
Lease liabilities, net of current portion | 19,844 | 19,225 | ||||||||||||||
Deferred revenue, net of current portion | 6,774 | 8,220 | ||||||||||||||
Total liabilities | 63,327 | 54,828 | ||||||||||||||
Commitments and contingencies | ||||||||||||||||
Stockholders' equity: | ||||||||||||||||
Convertible preferred stock | - | - | ||||||||||||||
Common stock | 20 | 18 | ||||||||||||||
Additional paid-in capital | 579,543 | 493,023 | ||||||||||||||
Accumulated other comprehensive gain | 7 | - | ||||||||||||||
Accumulated deficit | (371,615 | ) | (326,302 | ) | ||||||||||||
Total stockholders' equity | 207,955 | 166,739 | ||||||||||||||
Total liabilities and stockholders' equity | $ | 271,282 | $ | 221,567 | ||||||||||||
Gritstone Contacts
Media:
1AB
(973) 271-6085
dan@1abmedia.com
Investors:
tim@lifesciadvisors.com