Updated data from an ongoing randomized,
multi-center, placebo-controlled Phase 1 clinical trial of FT-4202
in sickle cell disease selected for an oral presentation
Forma Therapeutics Holdings, Inc. (Nasdaq: FMTX), a
clinical-stage biopharmaceutical company focused on rare
hematologic diseases and cancers, today announced that four
abstracts – including one oral presentation and three poster
presentations – have been accepted for presentation at the 62nd
American Society of Hematology (ASH) Virtual Annual Meeting taking
place December 5-8, 2020.
The oral presentation will feature clinical data from the
multiple ascending dose cohort of a randomized, multi-center,
placebo-controlled Phase 1 trial of FT-4202 in people living with
sickle cell disease (SCD). While the trial is currently enrolling
patients in the second dose escalation cohort of 600 mg FT-4202
daily, data will be presented on 9-12 patients who have completed
the 300 mg FT-4202 daily cohort. A “Trials in Progress” poster
presentation will highlight key aspects of the planned
registrational Phase 2/3 clinical trial. In addition, two
collaborative posters will report the findings of research of
FT-4202 in a mouse model of sickle cell anemia and in an ex vivo
analysis of blood samples from patients with SCD, respectively.
“We’re pleased the FT-4202 data have been selected for multiple
presentations at ASH 2020,” said Frank Lee, president and chief
executive officer of Forma. “Forma has a deep commitment to
advancing science in sickle cell disease. We look forward to
sharing data that will further characterize FT-4202 as an
investigational treatment for people living with sickle cell
disease.”
The abstracts, currently available on the ASH conference
website, are:
Oral Presentation
Title: FT-4202, an Allosteric Activator of Pyruvate
Kinase-R, Demonstrates Proof of Mechanism and Proof of Concept
after a Single Dose and after Multiple Daily Doses in a Phase 1
Study of Patients with Sickle Cell Disease
Date/Time: Monday, December 7, 2020 at 2:00 p.m. PT
Session: 114. Hemoglobinopathies, Excluding Thalassemia -
Clinical: Novel Treatments for Sickle Cell Disease Abstract:
679 Presenter: R. Clark Brown, MD, PhD, Pediatric
Hematologist/Oncologist, Medical Director of Sickle Cell at
Scottish Rite, Aflac Cancer and Blood Disorders Center of
Children’s Healthcare of Atlanta, and Associate Professor of
Pediatrics, Emory University School of Medicine
Poster Presentations
Title: An Adaptive, Randomized, Placebo-Controlled,
Double-Blind, Multi-Center Study of Oral FT-4202, a Pyruvate Kinase
Activator in Patients with Sickle Cell Disease (PRAISE)
Date: Monday, December 7, 2020 Session: 114.
Hemoglobinopathies, Excluding Thalassemia - Clinical: Poster III
Abstract: 2622 Presenter: Kenneth W. Wood, Executive
Director, Project Leadership at Forma Therapeutics, Inc.
Title: Oral Administration of FT-4202, an Allosteric
Activator of Pyruvate Kinase-R, Has Potent Anti-Sickling Effects in
a Sickle Cell Anemia (SCA) Mouse Model, Resulting in Improved RBC
Survival and Hemoglobin Levels
Date: Saturday, December 5, 2020 Session: 113.
Hemoglobinopathies, Excluding Thalassemia - New Genetic Approaches
to Sickle Cell Disease: Poster I Abstract: 784
Presenter: Archana Shrestha, PhD, Research Associate at
Cincinnati Children’s Hospital Medical Center
Title: Ex-Vivo FT-4202 Treatment Improves Hemoglobin
Oxygen Affinity and Membrane Health in Red Blood Cells of Patients
with Hemoglobin SS and Hemoglobin SC Disease Irrespective of Prior
Hydroxyurea Use
Date: Saturday, December 5, 2020 Session: 113.
Hemoglobinopathies, Excluding Thalassemia—New Genetic Approaches to
Sickle Cell Disease: Poster I Abstract: 786
Presenter: Diamantis Konstantinidis, Research Associate at
Cincinnati Children’s Hospital Medical Center
About Sickle Cell Disease
Sickle cell disease (SCD) is one of the most common disorders
caused by a single gene mutation. Prevalence of SCD is
approximately 100,000 people in the U.S. and approximately 30,000
people in France, Germany, Italy, Spain and the UK. While reporting
limitations complicate stating an exact number, the National
Institutes of Health reports that prevalence is estimated at over
20 million individuals worldwide. In people living with SCD, red
blood cells, or RBCs, spontaneously deform in low oxygen
conditions, taking on a sickle-like shape. Sickle cells are stiff
and have damaged membranes, causing the RBCs to clump and burst in
small blood vessels, resulting in inflammation and vaso-occlusive
crises. Repeated deformation also depletes the RBC energy supply,
called ATP. One important consequence of this energy depletion is
increased levels of a metabolite, 2,3-DPG, that further reduces the
RBCs’ affinity for oxygen and exacerbates the cycle of repeated
deformation and anemia.
About FT-4202
FT-4202 is a novel, oral, once-daily pyruvate kinase-R (PKR)
activator designed to be a disease-modifying therapy for the
treatment of sickle cell disease (SCD). Early studies and trials
have shown that FT-4202 works upstream by employing a multi-modal
approach and activating the red blood cells’ (RBC) natural PKR
activity to decrease 2,3-DPG levels, which we believe leads
hemoglobin to hold on to oxygen molecules longer to reduce RBC
sickling. FT-4202 has also shown downstream activity by increasing
ATP levels, the fuel that provides energy to cells, which we
believe may improve RBC health and survival. Together, these
effects have the potential to increase hemoglobin levels and
decrease painful vaso-occlusive crises. In preclinical safety
studies, FT-4202 did not inhibit aromatase activity, important
biological processes responsible for sexual development.
About Forma Therapeutics
Forma Therapeutics is a clinical-stage biopharmaceutical company
focused on the research, development and commercialization of novel
therapeutics to transform the lives of patients with rare
hematologic diseases and cancers. Our R&D engine combines deep
biology insight, chemistry expertise and clinical development
capabilities to create drug candidates with differentiated
mechanisms of action focused on indications with high unmet need.
Our work has generated a broad proprietary portfolio of programs
with the potential to provide profound patient benefit. For more
information, please visit www.FormaTherapeutics.com or follow us on
Twitter @FORMAInc and LinkedIn.
Forward-looking Statements
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of
1995, as amended, including, without limitation, express or implied
statements regarding FT-4202, our expectations of the therapeutic
benefits related thereto, the timing and success of ongoing
clinical trials, whether positive interim results from a clinical
study are predictive of the results of ongoing or future clinical
studies, and our growth as a company. The words “may,” “will,”
“could,” “would,” “should,” “expect,” “plan,” “anticipate,”
“intend,” “believe,” “estimate,” “predict,” “project,” “potential,”
“continue,” “target” and similar expressions are intended to
identify forward-looking statements, although not all
forward-looking statements contain these identifying words.
Any forward-looking statements in this press release are based
on management’s current expectations and beliefs and are subject to
a number of risks, uncertainties and important factors that may
cause actual events or results to differ materially from those
expressed or implied by any forward-looking statements contained in
this press release, including, without limitation, those risks and
uncertainties related to the advancement of our clinical programs
and other risks identified in our SEC filings, including those
risks discussed under the heading “Risk Factors” in our Quarterly
Report on Form 10-Q for the quarter ended June 30, 2020, as well as
other risks detailed in our subsequent filings with the SEC. We
caution you not to place undue reliance on any forward-looking
statements, which speak only as of the date they are made. We
disclaim any obligation to publicly update or revise any such
statements to reflect any change in expectations or in events,
conditions or circumstances on which any such statements may be
based, or that may affect the likelihood that actual results will
differ from those set forth in the forward-looking statements. Any
forward-looking statements contained in this press release
represent our views only as of the date hereof and should not be
relied upon as representing its views as of any subsequent date. We
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Media Contact: Kari Watson, +1 781-235-3060 MacDougall
kwatson@macbiocom.com Investor Contacts: Mario Corso, +1
781-366-5726 Forma Therapeutics mcorso@formatherapeutics.com
Stephanie Ascher, +1 212-362-1200 Stern Investor Relations
stephanie.ascher@sternir.com
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