Cogent Biosciences Provides Corporate Updates, Fourth Quarter and Full Year 2021 Financial Results
March 15 2022 - 7:00AM
Cogent Biosciences, Inc. (Nasdaq: COGT), a biotechnology
company focused on developing precision therapies for genetically
defined diseases, today announced financial results for the fourth
quarter and year ended December 31, 2021.
“In 2021, Cogent achieved substantial progress toward our goal
of establishing bezuclastinib as a best-in-class KIT mutant
inhibitor for systemic mastocytosis and gastrointestinal stromal
tumor (GIST) patients,” said Andrew Robbins, President and CEO of
Cogent Biosciences. “All three late-stage bezuclastinib clinical
trials are actively enrolling patients, and we look forward to
presenting initial clinical data from APEX in the first half of
2022. In addition, we are excited about the progress the Cogent
Research Team has made to date and look forward to sharing further
details on bezuclastinib, as well as our growing portfolio, at our
upcoming R&D Investor Event.”
Key Clinical, Research and Corporate
Highlights
- Cogent’s highly potent and selective KIT mutant
inhibitor, bezuclastinib, is now under investigation in three
late-stage clinical trials:
- APEX: on track for initial clinical data readout in the
first half of 2022Cogent is currently enrolling APEX, a
global, multicenter, Phase 2 clinical trial of bezuclastinib in
patients with Advanced Systemic Mastocytosis (AdvSM) and expects to
report initial clinical data at a scientific conference during the
first half of 2022, including levels of serum tryptase, a validated
biomarker of mast cell activity. Learn more about the APEX trial
at cogentclinicaltrials.com/APEX.
- SUMMIT: initiated in patients with Nonadvanced Systemic
Mastocytosis (NonAdvSM) Cogent is currently enrolling
SUMMIT, a randomized, double-blind, placebo-controlled, global,
multicenter, Phase 2 clinical trial. The study is designed to
explore the safety and efficacy of bezuclastinib in patients with
moderate to severe Indolent Systemic Mastocytosis (ISM) or
Smoldering Systemic Mastocytosis (SSM). Learn more about the SUMMIT
trial at cogentclinicaltrials.com/SUMMIT.
- PEAK: initiated in patients with Gastrointestinal
Stromal Tumors (GIST)During the fourth quarter of 2021,
Cogent initiated and now is currently enrolling PEAK, a randomized,
open-label, global, Phase 3 clinical trial. The PEAK study is
designed to explore the efficacy of bezuclastinib in combination
with sunitinib compared to sunitinib alone in patients with locally
advanced, unresectable or metastatic GIST who have received prior
treatment with imatinib. Learn more about the PEAK trial at
cogentclinicaltrials.com/PEAK.
- Preclinical data presented during the third quarter of
2021 highlights bezuclastinib as a potent KIT inhibitor with
minimal CNS penetration and which avoids PDGFR inhibition:
- Cogent presented preclinical data providing further evidence of
bezuclastinib as a differentiated, potent, and selective KIT mutant
inhibitor with minimal brain penetration while avoiding inhibition
of PDGFR isoforms. These data were presented in a virtual poster at
the 2021 AACR-NCI-EORTC Virtual International Conference on
Molecular Targets and Cancer Therapeutics.
- Cogent Research Team created to generate robust
pipeline of potential best-in-class small molecules
- Cogent Research Team: In 2021, we founded a
highly-experienced Boulder-based discovery and research team
focused on pioneering best-in-class, small molecule therapeutics to
expand Cogent's pipeline. John Robinson, PhD, leads the Cogent
Research Team, which has grown to over 35 employees and will move
into its newly-built, state-of-the-art research facility in Boulder
this spring.
- R&D Investor Event: Cogent will host an
R&D Investor Event at which the Cogent Research Team will share
additional nonclinical data demonstrating bezuclastinib’s potential
as a best-in-class KIT mutant inhibitor, outline its strategy and
focus to create best-in-class small molecules, and present early
data from its growing pipeline of novel, small molecule targeted
therapy programs including FGFR2. The R&D Investor Event will
be a live webcast on Friday, April 8, 2022 beginning at 4:05 p.m.
ET. On the day of the webcast, the American Association for Cancer
Research (AACR) poster presentations will be made available through
the AACR conference website at 1:00 p.m. ET. Additional details
about the R&D Investor Event will be shared in the coming
weeks.
- Successfully bolstered Cogent balance sheet utilizing
our At-The-Market (ATM) Program: In Q4 2021, pursuant to
Cogent’s ATM program, we completed the sale of common shares to
certain institutional investors for net proceeds of approximately
$38 million with offering prices ranging between $9.25 and $10.30
per share.
- Appointed Zamaneh Mikhak, MD as Senior Vice
President, Head of Clinical Development
- Dr. Mikhak joins as an allergist/immunologist and physician
scientist with over 20 years of experience in clinical practice and
basic and translational research. Prior to joining Cogent, she
held several leadership roles with increasing responsibilities,
most recently leading clinical stage programs at both Boston
Pharmaceuticals and Kiniksa Pharmaceuticals. Dr. Mikhak was an
Assistant Professor at Harvard Medical School and an NIH funded
Principal Investigator at Massachusetts General Hospital prior to
joining industry. She earned her MD from the Perelman School
of Medicine at the University of Pennsylvania and her Bachelor of
Arts degree in Biology from Boston University.
- Appointed Lei Sun, PhD as Vice President,
Clinical Pharmacology & Translational Medicine
- Dr. Sun joins with over 20 years of industry experience with
demonstrated leadership in clinical pharmacology, translational
medicine, and DMPK in multiple therapeutic areas. Prior to
joining Cogent, she was Head of Clinical Pharmacology at Alkermes.
Earlier in her career, Dr. Sun held several roles of increasing
responsibility at Ziopharm Oncology, Alnylam Pharmaceuticals, and
Wyeth/Pfizer. Dr. Sun received her PhD in Chemistry & Chemical
Biology and MS in Chemical & Biochemical Engineering from
Rutgers University and her BS in Material Sciences &
Engineering from Tianjin University in China.
- Appointed Lora Marden as Vice President, Patient
Advocacy, Engagement and Innovation
- Ms. Marden joins with over 15 years of rare disease
biopharmaceutical and social services experience. Prior to joining
Cogent, Ms. Marden was the Head of Global Patient Advocacy &
Engagement at Kiniksa Pharmaceuticals. Previously, she held roles
of increasing leadership responsibility in the areas of marketing,
patient advocacy, medical affairs, commercial operations, and
patient services at Sanofi-Genzyme, Alnylam Pharmaceuticals, and
Sobi Inc., including contributing to the launch of multiple rare
disease therapies. She currently sits as a Board Member for the
MassBioEd Foundation and holds a Bachelor of Arts in Psychology
from the University of Rochester.
Fourth Quarter and Year End 2021 Summarized Financial
Results
- R&D Expenses: Research
and development expenses were $20.5 million for the fourth quarter
of 2021 and $55.9 million for the year ended December 31, 2021, as
compared to $6.1 million for the fourth quarter of 2020 and $25.7
million for the year ended December 31, 2020. These expenses
included trial start-up costs associated with SUMMIT and
PEAK and initial costs related to expanding the Cogent
Research Team.
- G&A Expenses: General and
administrative expenses were $5.1 million for the fourth quarter of
2021 and $19.6 million for the year ended December 31, 2021, as
compared to $5.3 million for the fourth quarter of 2020 and $17.4
million for the year ended December 31, 2020.
- Net Loss: Net loss was $24.9 million for
the fourth quarter of 2021 and $72.3 million for the year ended
December 31, 2021, as compared to a net loss of $11.3 million for
the fourth quarter of 2021 and $74.8 million for the year ended
December 31, 2020.
- Cash and Cash Equivalents: As
of December 31, 2021, Cogent had cash and cash equivalents
of $219.7 million. The company believes that its cash and cash
equivalents will be sufficient to fund its operating expenses and
capital expenditure requirements into 2024.
About Cogent Biosciences, Inc. Cogent
Biosciences is a biotechnology company focused on developing
precision therapies for genetically defined diseases. The most
advanced clinical program, bezuclastinib, is a selective tyrosine
kinase inhibitor that is designed to potently inhibit the KIT D816V
mutation as well as other mutations in KIT exon 17. KIT D816V is
responsible for driving systemic mastocytosis, a serious disease
caused by unchecked proliferation of mast cells. Exon 17 mutations
are also found in patients with advanced gastrointestinal stromal
tumors (GIST), a type of cancer with strong dependence on oncogenic
KIT signaling. In addition to bezuclastinib, the Cogent Research
Team is developing a portfolio of novel targeted therapies to help
patients fighting serious, genetically driven diseases. Cogent
Biosciences is based in Cambridge, MA and Boulder, CO. Visit our
website for more information at www.cogentbio.com. Follow Cogent
Biosciences on social media: Twitter and LinkedIn. Information that
may be important to investors will be routinely posted on our
website and Twitter.
Forward Looking StatementsThis press release
contains forward-looking statements within the meaning of the
Private Securities Litigation Reform Act of 1995, including, but
not limited to, statements regarding the company’s anticipated cash
runway, the expectation to present preliminary clinical data from
APEX in the first half of 2022, the company’s planned R&D
investor event in April 2022, the anticipated move for
the Cogent Research Team into its newly-built, state-of-the-art
research facility in Boulder this spring, and the expectation that
the company’s AACR poster presentations will be made available
through the AACR conference website on schedule. The use of words
such as, but not limited to, "anticipate," "believe," "continue,"
"could," "estimate," "expect," "intend," "may," "might," "plan,"
"potential," "predict," "project," "should," "target," "will," or
"would" and similar words expressions are intended to identify
forward-looking statements. Forward-looking statements are neither
historical facts nor assurances of future performance. Instead,
they are based on our current beliefs, expectations and assumptions
regarding the future of our business, future plans and strategies,
our clinical results, the rate of enrollment in our clinical trials
and other future conditions. New risks and uncertainties may emerge
from time to time, and it is not possible to predict all risks and
uncertainties. No representations or warranties (expressed or
implied) are made about the accuracy of any such forward-looking
statements. We may not actually achieve the forecasts or milestones
disclosed in our forward-looking statements, and you should not
place undue reliance on our forward-looking statements. Such
forward-looking statements are subject to a number of material
risks and uncertainties including but not limited to those set
forth under the caption "Risk Factors" in Cogent's most recent
Annual Report on Form 10-K filed with the SEC, as well as
discussions of potential risks, uncertainties, and other important
factors in our subsequent filings with the SEC. Any
forward-looking statement speaks only as of the date on which it
was made. Neither we, nor our affiliates, advisors or
representatives, undertake any obligation to publicly update or
revise any forward-looking statement, whether as result of new
information, future events or otherwise, except as required by law.
These forward-looking statements should not be relied upon as
representing our views as of any date subsequent to the date
hereof.
COGENT BIOSCIENCES, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS (in
thousands) (unaudited)
|
|
Three Months Ended December 31, |
|
|
Year Ended December 31, |
|
|
|
2021 |
|
|
2020 |
|
|
2021 |
|
|
2020 |
|
Collaboration revenue |
|
$ |
— |
|
|
$ |
— |
|
|
$ |
— |
|
|
$ |
7,871 |
|
Operating expenses: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Research and development |
|
|
20,514 |
|
|
|
6,107 |
|
|
|
55,913 |
|
|
|
25,738 |
|
General and administrative |
|
|
5,125 |
|
|
|
5,348 |
|
|
|
19,638 |
|
|
|
17,422 |
|
Acquired in-process research and development |
|
|
— |
|
|
|
— |
|
|
|
— |
|
|
|
46,910 |
|
Total operating expenses |
|
|
25,639 |
|
|
|
11,455 |
|
|
|
75,551 |
|
|
|
90,070 |
|
Loss from operations |
|
|
(25,639 |
) |
|
|
(11,455 |
) |
|
|
(75,551 |
) |
|
|
(82,199 |
) |
Other income: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Interest income |
|
|
106 |
|
|
|
70 |
|
|
|
467 |
|
|
|
144 |
|
Gain on disposal of long-lived assets |
|
|
— |
|
|
|
31 |
|
|
|
— |
|
|
|
7,493 |
|
Other income |
|
|
621 |
|
|
|
531 |
|
|
|
2,468 |
|
|
|
779 |
|
Change in fair value of CVR liability |
|
|
— |
|
|
|
(516 |
) |
|
|
343 |
|
|
|
(1,025 |
) |
Total other income |
|
|
727 |
|
|
|
116 |
|
|
|
3,278 |
|
|
|
7,391 |
|
Net loss |
|
$ |
(24,912 |
) |
|
$ |
(11,339 |
) |
|
$ |
(72,273 |
) |
|
$ |
(74,808 |
) |
COGENT BIOSCIENCES, INC.
SELECTED CONDENSED CONSOLIDATED BALANCE
SHEET DATA(in thousands) (unaudited)
|
|
December 31, |
|
|
December 31, |
|
|
|
2021 |
|
|
2020 |
|
Cash and cash equivalents |
|
$ |
219,684 |
|
|
$ |
242,190 |
|
Working Capital |
|
$ |
205,556 |
|
|
$ |
231,818 |
|
Total assets |
|
$ |
232,092 |
|
|
$ |
250,916 |
|
Total liabilities |
|
$ |
17,908 |
|
|
$ |
16,249 |
|
Total stockholders’ equity |
|
$ |
214,184 |
|
|
$ |
234,667 |
|
|
|
|
|
|
|
|
|
|
MEDIA CONTACT:
Amanda Sellers
asellers@vergescientific.com
Cogent Biosciences (NASDAQ:COGT)
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