Gritstone bio Reports Second Quarter 2024 Financial Results and Provides Corporate Updates
August 13 2024 - 4:05PM
Gritstone bio, Inc. (Nasdaq: GRTS), a clinical-stage biotechnology
company working to develop the world’s most potent vaccines, today
reported financial results for the second quarter ended June 30,
2024 and provided recent corporate and clinical updates.
“This is an exciting time for Gritstone, as we are on the cusp
of unlocking important data about our promising new therapeutic
modality in front-line metastatic microsatellite-stable colorectal
cancer (MSS-CRC),” said Andrew Allen, MD, PhD, Co-founder,
President & CEO of Gritstone bio. “Up to 95% of patients with
metastatic CRC, the second most common cause of cancer death, are
MSS. Delivering a new treatment option to these patients, who do
not benefit from today’s immunotherapies, would be transformative.
The emerging progression-free survival (PFS) benefit we reported in
April is highly encouraging, especially in this tough to treat
patient population. We have waited for these clinical data to
mature and look forward to sharing the updated dataset next month.
If we continue to see evidence of a clinical benefit with GRANITE,
as measured by PFS, we believe new hope can be brought to patients
who have not been helped by immune checkpoint blockade.”
Dr. Allen added, "Along with advancing GRANITE in CRC, our team
continues to innovate across our programs, reinforcing the
potential of our underlying technologies. Our recent AACR
presentation highlights the unique power of EDGE™, our proprietary
neoantigen identification platform that underpins all our programs.
Our recent presentation at ESCMID showcases the ability of our
self-amplifying mRNA vector (samRNA) to induce long-lasting immune
responses. Gritstone remains uniquely positioned to deliver on the
promise of next-generation vaccine technologies to prevent, treat
and eradicate disease.”
Corporate Updates
- In April 2024, Gritstone completed an underwritten public
offering resulting in gross proceeds of $32.5 million.
- In April 2024, Gritstone appointed Stephen Webster to its Board
of Directors. A veteran finance executive with over 30 years in the
biotechnology industry, Mr. Webster has held several key roles and
been involved in multiple strategic transactions. Mr. Webster was
the Chief Financial Officer of Spark Therapeutics from July 2014
until its acquisition by Roche for $4.3 billion in December
2019.
- In July 2024, Gritstone bio engaged the Colorectal Cancer
Alliance and the Paltown Development Foundation 501(c)(3), the
fiduciary for Colontown.org, as part of its effort to educate and
empower patients living with colorectal cancer and their
caregivers.
- In August 2024, Gritstone bio held a virtual KOL event to
discuss the unmet need and potential role of GRANITE in metastatic
microsatellite-stable colorectal cancer (MSS-CRC). The event
featured J. Randolph Hecht, MD, Professor of Clinical Medicine and
Director of the UCLA GI Oncology Program, and Howard Brown, CRC
Survivor, Patient and Advocate. Details here.
Clinical Program Updates Tumor-Specific
Neoantigen Oncology Programs (GRANITE and SLATE)GRANITE –
Personalized neoantigen vaccine programSLATE – “Off-the-shelf”
neoantigen vaccine program
- Preliminary results (reported April 1, 2024) from the
ongoing randomized Phase 2 study suggest GRANITE could drive
meaningful clinical benefit in front-line metastatic
microsatellite-stable colorectal cancer (MSS-CRC). Gritstone
expects to report mature progression-free survival (PFS) data in 3Q
2024.
- Preliminary data, while immature, showed a trend of extended
PFS in GRANITE-treated vs. control patients.
- Hazard ratio of 0.82 (18% relative risk reduction of
progression or death with GRANITE vs. control) in the overall
population, where clinical data are less mature ([95% CI,
0.34-1.67]; 62% censored)
- Hazard ratio of 0.52 (48% relative risk reduction of
progression or death with GRANITE vs. control) in a
fast-progressor, i.e. ‘high-risk’ group1, where clinical data are
more mature ([95% CI, 0.15-1.38]; 44% censored). Too few events in
the slow-progressor group at this early look to draw any efficacy
conclusions.1Fast-progressor subgroup defined as baseline ctDNA
above the median value (2%) for the control group (ctDNA quantified
as mean variant allele frequency [VAF] at time of study
randomization).
- Long-term circulating tumor DNA (ctDNA) data aligned with PFS
trend and favored GRANITE vs. control patients
- EDGE™ predicts HLA Class I presentation with >80%
accuracy. In April 2024, Gritstone presented an update on
the predictive performance of both HLA Class I and HLA Class II
presentation at the 2024 American Association for Cancer Research
(AACR) Annual Meeting in San Diego, CA. The findings further
Gritstone’s belief that EDGE is leading the field in neoantigen
prediction.
- The clinical trial collaboration with the National
Cancer Institute (NCI) to evaluate an autologous mutant
KRAS-directed TCR-T cell therapy in combination with SLATE-KRAS,
Gritstone’s KRAS-directed “off-the-shelf” vaccine candidate, is
ongoing. The study is led by Steven A. Rosenberg, M.D.,
Ph.D., Chief of the Surgery Branch at the NCI's Center for Cancer
Research and builds into the growing interest in combining
tumor-antigen specific cell therapy with matched vaccines.
Infectious Disease ProgramsCORAL –
Next-generation SARS-CoV-2 vaccine program that serves as
proof-of-concept for Gritstone’s samRNA platform and novel approach
in infectious diseases
- Efforts to initiate a head-to-head Phase 2b study of
Gritstone’s next-generation COVID-19 vaccine (the CORAL Phase 2b
study) per the Biomedical Advanced Research and Development
Authority (BARDA)2 contract
continue. Gritstone will provide further updates as it is
able.
- Follow up data from the Phase 1 CORAL study highlight
the durability and potential broad utility of Gritstone’s samRNA
COVID-19 vaccine. In April 2024, Gritstone presented
12-month follow up data from the Phase 1 CORAL-CEPI at ESCMID 2024.
The results reinforced previous findings showing induction of broad
and durable immune responses through 12 months.
HIV – Collaboration with Gilead to research and develop
vaccine-based HIV immunotherapy treatment
- The collaboration with Gilead to research and develop a
vaccine-based HIV immunotherapy treatment continues under Gilead’s
direction.
Second Quarter 2024 Financial Results
- Cash, cash equivalents, marketable securities and
restricted cash were $61.7 million as of June 30, 2024,
compared to $52.8 million as of March 31, 2024.
- Research and development expenses were $20.8
million for the three months ended June 30, 2024, compared to $31.0
million for the three months ended June 30, 2023. The decrease of
$10.2 million for the three months ended June 30, 2024, compared to
the three months ended June 30, 2023 was primarily due to decreases
of $3.2 million in personnel-related expenses, $3.2 million in
laboratory supplies, $2.6 million in outside services, consisting
primarily of clinical trial and other chemistry, manufacturing and
controls related expenses and $1.2 million in facilities related
costs.
- General and administrative expenses were $7.7
million for the three months ended June 30, 2024, compared to $6.7
million for the three months ended June 30, 2023. The increase of
$1.0 million was primarily attributable to increases of $0.9
million in personnel-related expenses, including a $0.5 million
increase of non-cash stock-based compensation, and $0.1 million in
facilities related costs.
- Grant revenues were $0.9 million for the three
months ended June 30, 2024. During the three months ended June 30,
2024, we recorded $0.9 million in grant revenue from CEPI.
2
This project has been supported in whole or in part with federal
funds from the Department of Health and Human Services;
Administration for Strategic Preparedness and Response; Biomedical
Advanced Research and Development Authority (BARDA), under contract
number 75A50123C00062. |
|
About Gritstone bioGritstone bio, Inc. (Nasdaq:
GRTS) is a clinical-stage biotechnology company that aims to
develop the world’s most potent vaccines. We leverage our
innovative vectors and payloads to train multiple arms of the
immune system to attack critical disease targets. Independently and
with our collaborators, we are advancing a portfolio of product
candidates to treat and prevent viral diseases and solid tumors in
pursuit of improving patient outcomes and eliminating disease.
www.gritstonebio.com
Gritstone Forward-Looking StatementsThis
press release contains forward-looking statements, including, but
not limited to, statements related to our clinical and regulatory
development plans for our product candidates; our expectations
regarding the data to be derived in our ongoing and planned
clinical trials; the timing of commencement of our future
nonclinical studies, clinical trials and research and development
programs; our ability to discover, develop and advance product
candidates into, and successfully complete, clinical trials; and
our plans and strategy regarding maintaining existing and entering
into new collaborations and/or partnerships. 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’ clinical 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. 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 Annual Report on Form 10-K filed on March 5, 2024 and
any subsequent current and periodic reports filed with the
Securities and Exchange Commission.
This press release concerns drugs that are under clinical
investigation, and which have not yet been approved for marketing
by the U.S. Food and Drug Administration. They are currently
limited by Federal law to investigational use, and no
representation is made as to their safety or effectiveness for the
purposes for which they are being investigated.
Gritstone ContactsInvestors:George E.
MacDougallGritstone bio, Inc.ir@gritstone.com
Media:Dan Budwick1AB(973) 271-6085dan@1abmedia.com
Gritstone bio,
Inc.Condensed Consolidated Balance Sheets
(unaudited)(In thousands)
|
|
June 30, 2024 |
|
December 31, 2023 |
Assets |
|
|
|
|
Current assets: |
|
|
|
|
Cash and cash equivalents |
|
$ |
50,900 |
|
|
$ |
62,986 |
|
Marketable securities |
|
|
4,812 |
|
|
|
16,288 |
|
Restricted cash |
|
|
1,274 |
|
|
|
2,299 |
|
Prepaid expenses and other current assets |
|
|
3,724 |
|
|
|
5,862 |
|
Total current assets |
|
|
60,710 |
|
|
|
87,435 |
|
Long-term restricted cash |
|
|
4,695 |
|
|
|
5,290 |
|
Property and equipment,
net |
|
|
12,527 |
|
|
|
17,281 |
|
Lease right-of-use assets |
|
|
64,001 |
|
|
|
66,839 |
|
Deposits and other long-term
assets |
|
|
609 |
|
|
|
924 |
|
Total assets |
|
$ |
142,542 |
|
|
$ |
177,769 |
|
Liabilities and
stockholders’ equity |
|
|
|
|
Current liabilities: |
|
|
|
|
Accounts payable |
|
$ |
4,132 |
|
|
$ |
3,819 |
|
Accrued compensation |
|
|
5,272 |
|
|
|
9,357 |
|
Accrued liabilities |
|
|
856 |
|
|
|
1,213 |
|
Accrued research and development expenses |
|
|
3,002 |
|
|
|
3,696 |
|
Lease liabilities, current portion |
|
|
7,159 |
|
|
|
6,904 |
|
Deferred revenue, current portion |
|
|
698 |
|
|
|
2,350 |
|
Warrant liability |
|
|
2,782 |
|
|
|
— |
|
Total current liabilities |
|
|
23,901 |
|
|
|
27,339 |
|
Other liabilities,
noncurrent |
|
|
1,117 |
|
|
|
709 |
|
Lease liabilities, net of
current portion |
|
|
54,829 |
|
|
|
57,727 |
|
Debt, noncurrent |
|
|
40,506 |
|
|
|
40,144 |
|
Total liabilities |
|
|
120,353 |
|
|
|
125,919 |
|
Stockholders’ equity: |
|
|
|
|
Preferred stock |
|
|
— |
|
|
|
— |
|
Common stock |
|
|
24 |
|
|
|
22 |
|
Additional paid-in capital |
|
|
745,510 |
|
|
|
711,386 |
|
Accumulated other comprehensive (loss) gain |
|
|
(3 |
) |
|
|
3 |
|
Accumulated deficit |
|
|
(723,342 |
) |
|
|
(659,561 |
) |
Total stockholders’
equity |
|
|
22,189 |
|
|
|
51,850 |
|
Total liabilities and
stockholders’ equity |
|
$ |
142,542 |
|
|
$ |
177,769 |
|
|
|
|
|
|
|
|
|
|
Gritstone bio,
Inc.Condensed Consolidated Statements of
Operations and Comprehensive Loss (unaudited)(In
thousands, except share and per share amounts)
|
|
Three Months Ended June 30, |
|
Six Months Ended June 30, |
|
|
|
2024 |
|
|
|
2023 |
|
|
|
2024 |
|
|
|
2023 |
|
Revenues: |
|
|
|
|
|
|
|
|
Collaboration and license revenues |
|
$ |
57 |
|
|
$ |
400 |
|
|
$ |
106 |
|
|
$ |
941 |
|
Grant revenues |
|
|
864 |
|
|
|
1,555 |
|
|
|
2,557 |
|
|
|
3,456 |
|
Total revenues |
|
|
921 |
|
|
|
1,955 |
|
|
|
2,663 |
|
|
|
4,397 |
|
Operating expenses: |
|
|
|
|
|
|
|
|
Research and development |
|
|
20,811 |
|
|
|
30,967 |
|
|
|
53,852 |
|
|
|
61,481 |
|
General and administrative |
|
|
7,698 |
|
|
|
6,716 |
|
|
|
16,200 |
|
|
|
13,461 |
|
Total operating expenses |
|
|
28,509 |
|
|
|
37,683 |
|
|
|
70,052 |
|
|
|
74,942 |
|
Loss from operations |
|
|
(27,588 |
) |
|
|
(35,728 |
) |
|
|
(67,389 |
) |
|
|
(70,545 |
) |
Interest income |
|
|
691 |
|
|
|
1,479 |
|
|
|
1,403 |
|
|
|
3,157 |
|
Interest expense |
|
|
(1,304 |
) |
|
|
(985 |
) |
|
|
(2,600 |
) |
|
|
(1,828 |
) |
Other income (expense) |
|
|
4,805 |
|
|
|
(22 |
) |
|
|
4,805 |
|
|
|
(22 |
) |
Net loss |
|
|
(23,396 |
) |
|
|
(35,256 |
) |
|
|
(63,782 |
) |
|
|
(69,238 |
) |
Other comprehensive loss: |
|
|
|
|
|
|
|
|
Unrealized loss on marketable securities |
|
|
(2 |
) |
|
|
(73 |
) |
|
|
(6 |
) |
|
|
(45 |
) |
Comprehensive loss |
|
$ |
(23,398 |
) |
|
$ |
(35,329 |
) |
|
$ |
(63,787 |
) |
|
$ |
(69,283 |
) |
Net loss per share, basic and
diluted |
|
$ |
(0.16 |
) |
|
$ |
(0.31 |
) |
|
$ |
(0.49 |
) |
|
$ |
(0.60 |
) |
Weighted-average number of
shares used in computing net loss per share, basic and diluted |
|
|
143,296,662 |
|
|
|
114,929,523 |
|
|
|
130,843,943 |
|
|
|
114,676,261 |
|
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