- Biohaven's first-in-class Molecular Degrader of Extracellular
Proteins (MoDE™) technology targeting IgG removal, BHV-1300, was
selected for an oral presentation at AAN highlighting its novel
mechanism of action and the latest preclinical data demonstrating
rapid, robust, and selective target removal
- Biohaven announces it will present safety and IgG lowering data
from its ongoing single ascending dose (SAD) study of BHV-1300 at
the company's annual R&D day at the Yale Innovation Summit in
New Haven, Connecticut on
May 29, 2024
- Safety, tolerability, and target engagement data showing the
differentiated profile of BHV-7000 as a potential best-in-class Kv7
activator will be presented as both oral and poster presentations;
the Phase 2/3 focal epilepsy program is now enrolling patients
- AAN Abstract of Distinction awarded to BHV-2100, which
demonstrated potent reversal of pain in preclinical models and
favorable initial safety and pharmacokinetic data in Phase 1
studies, highlighting the potential for TRPM3 antagonism as a novel
nonopioid target to treat pain and migraine
- Oral and poster presentations of troriluzole as a novel
glutamate modulating agent with favorable pharmacokinetics, safety,
and outcomes data in the potential treatment of neurologic and
neuropsychiatric disorders
- Biohaven announces the Data Monitoring Committee for its Phase
3 trial in obsessive-compulsive disorder convened in the second
quarter to review the interim analysis and informed the Company
that the study may continue
- Additional efficacy and safety data regarding troriluzole in
spinocerebellar ataxia will also be presented in both oral and
poster format
- Poster presentation of RESILIENT Phase 3 study design with
taldefgrobep alfa in spinal muscular atrophy; study completed
enrollment and topline results anticipated in the second half of
2024
- Biohaven announces the FDA granted "rare pediatric disease"
designation for taldefgrobep alfa thereby providing the potential
to receive a priority review voucher (PRV) if ultimately approved
for the indication of spinal muscular atrophy
- Other presentations and posters include development of the
PARCOMS, a new outcome measure for Parkinson's disease clinical
trials, application of machine learning in video assessment of
gait, and data demonstrating a reduced risk for Parkinson's disease
in patients taking anti-inflammatory agents
- Three oral presentations and 6 poster presentations from the
Biohaven Clinical and Health Outcomes group describe the
development and validation of novel scales and natural history
studies in support of troriluzole and BHV-8000 development
programs, the impact of immune-modulating therapy in Parkinson's
disease, the burden of illness in focal epilepsy and KCNQ2-DEE
(BHV-7000), and the application of AI machine learning technology
to quantify patient mobility with troriluzole in spinocerebellar
ataxia
DENVER,
CO and NEW HAVEN,
Conn., April 13, 2024 /PRNewswire/ -- Biohaven
Ltd. (NYSE: BHVN) announced today that 20 abstracts, including
8 oral presentations and 12 posters, will be featured this weekend
starting April 13th at the
2024 American Academy of Neurology (AAN) Annual Meeting, taking
place in Denver, Colorado. The
presentations highlight Biohaven's leadership in neuroscience and
extensive development programs evaluating novel therapies to treat
neurological diseases, with abstracts covering programs that
include Kv7 ion channel modulation, molecular degraders of
extracellular protein (MoDEs), TRPM3 antagonism, TYK2/JAK1
inhibition, glutamate modulation, and myostatin inhibition.

Irfan Qureshi, M.D., Chief
Medical Officer of Biohaven, commented, "The research being
presented at the AAN Annual Meeting emphasizes Biohaven's
commitment to developing new therapeutic options across a range of
neurological diseases. By targeting novel mechanisms of action,
differentiated from currently available treatments and other
therapies in development, and following innovative science,
Biohaven continues to strive for better treatments for people
living with neurological disorders. We are particularly honored
that the AAN Science Committee selected our BHV-2100 (TRPM3)
abstract as an AAN Abstract of Distinction, recognizing it as the
top abstract in the pain category. Following the completion of
Phase 1 studies in the first half of 2024, we look forward to
initiating a Phase 2 study with BHV-2100 in migraine in the second
half of the year and are excited by the potential for this novel
nonopioid approach to treat pain."
Vlad Coric M.D., Chief Executive
Officer and Chairman of Biohaven, added, "Our leadership in
neuroscience research is on full display at the AAN Annual Meeting
with the breadth and depth of clinical, epidemiological, and
preclinical programs highlighted in our scientific presentations.
Central nervous system (CNS) disorders continue to represent one of
the highest unmet medical needs facing our society and we must act
urgently to bring better treatments to patients and improve
clinical outcomes. We believe that the next generation of therapies
for CNS disorders will include MoDEs for autoimmune disorders, ion
channel modulation for epilepsy, migraine and other pain disorders,
immune modulation for neurodegenerative disorders including
Parkinson's and Alzheimer's diseases, myostatin targeting drugs for
neuromuscular disorders and glutamate modulating agents for
neuropsychiatric disorders. I am so proud of the team at Biohaven
who are working tirelessly to alleviate the burden of these
devastating disorders."
The complete list of Biohaven's accepted abstract titles is
below. Full abstracts can be viewed online at
https://index.mirasmart.com/AAN2024/.
Oral Presentations:
- Novel Bispecific Degrader BHV-1300 Achieves Rapid, Robust, and
Selective IgG Reduction in Preclinical Models Including Nonhuman
Primates
- BHV-2100, a First-in-class TRPM3 Antagonist for the Treatment
of Pain (AAN Abstract of Distinction)
- Characterization of BHV-7000: A Novel Kv7.2/7.3 Activator for
the Treatment of Seizures
- Association of Anti-inflammatory Therapy Use with the Incidence
of Parkinson's Disease: A Person-Time Analysis Among Patients with
Autoimmune Diseases
- Re-weighting MDS-UPDRS Motor Items for Optimal Sensitivity to
Parkinson's Disease Progression in Untreated Patients Using
Parkinson's Progression Markers Initiative Data
- Population Pharmacokinetic Modeling of Riluzole After
Administration of a Next Generation Prodrug Troriluzole
- Next Generation Prodrug Troriluzole: Increased Bioavailability
of Riluzole with No Food Effect in Healthy Subjects
- Matching-adjusted Indirect Comparison of Troriluzole Versus
Untreated Natural History Cohort in Spinocerebellar Ataxia
Poster Presentations:
- Phase 1 Study Evaluating the Safety and Tolerability of
BHV-7000, a Novel, Selective Kv7.2/7.3 Potassium Channel Activator,
in Healthy Adults
- Novel, Selective Kv7.2/7.3 Potassium Channel Activator,
BHV-7000, Demonstrates Dose-dependent Pharmacodynamic Effects on
EEG Parameters in Healthy Adults
- Determinants of Health-related Quality of Life of Patients with
Focal Epilepsy: A Systematic Literature Review
- Functional Impairments in Patients with KCNQ2-DEE: Associations
Among Key Clinical Features
- The Phase 3 RESILIENT Study: Taldefgrobep Alfa in Spinal
Muscular Atrophy
- Re-weighting MDS-UPDRS Part II Items for Optimal Sensitivity to
Parkinson's Disease Progression Using Parkinson's Progression
Markers Initiative Natural History Data
- Safety, Tolerability, and Pharmacokinetics of Single and
Multiple Rising Doses of a Next Generation Prodrug Troriluzole in
Healthy Subjects
- Troriluzole Exhibits Favorable Hepatic Safety Profile Across a
Diverse Range of Disorders
- No Clinically Relevant Effects of Hepatic Impairment on the
Pharmacokinetics of a Next Generation Prodrug Troriluzole
- Automated Video-based Characterization of Movement Quality in a
Phase III Clinical Trial of Troriluzole in Subjects with
Spinocerebellar Ataxia
- Psychometric Validation of the Modified-functional Scale for
the Assessment and Rating of Ataxia
- Development of a Novel Composite Measure (SCACOMS) to Assess
Disease Progression in Spinocerebellar Ataxia
Posters and presentations will be available on
the Posters and Presentations page after the
conference at www.biohaven.com.
About Biohaven
Biohaven is a biopharmaceutical
company focused on the discovery, development, and
commercialization of life-changing treatments in key therapeutic
areas, including immunology, neuroscience, and oncology. The
company is advancing its innovative portfolio of therapeutics,
leveraging its proven drug development experience and multiple
proprietary drug development
platforms. Biohaven's extensive clinical and preclinical
programs include Kv7 ion channel modulation for epilepsy and mood
disorders; extracellular protein degradation for immunological
diseases; TRPM3 antagonism for migraine and neuropathic pain;
TYK2/JAK1 inhibition for neuroinflammatory disorders; glutamate
modulation for OCD and SCA; myostatin inhibition for neuromuscular
and metabolic diseases, including SMA and obesity; and antibody
recruiting, bispecific molecules and antibody drug conjugates for
cancer.
Forward-looking Statements
This news release includes
forward-looking statements within the meaning of the Private
Securities Litigation Reform Act of 1995. The use of certain words,
including "continue", "plan", "will", "believe", "may", "expect",
"anticipate" and similar expressions, is intended to identify
forward-looking statements. Investors are cautioned that any
forward-looking statements, including statements regarding the
future development, timing and potential marketing approval and
commercialization of development candidates, are not guarantees of
future performance or results and involve substantial risks and
uncertainties. Actual results, developments and events may differ
materially from those in the forward-looking statements as a result
of various factors including: the expected timing, commencement and
outcomes of Biohaven's planned and ongoing clinical
trials; the timing of planned interactions and filings with the
FDA; the timing and outcome of expected regulatory filings;
complying with applicable U.S. regulatory requirements;
the potential commercialization of Biohaven's product
candidates; the potential for Biohaven's product
candidates to be first in class therapies; and the effectiveness
and safety of Biohaven's product candidates. Additional
important factors to be considered in connection with
forward-looking statements are described
in Biohaven's filings with the Securities and
Exchange Commission, including within the sections titled "Risk
Factors" and "Management's Discussion and Analysis of Financial
Condition and Results of Operations". The forward-looking
statements are made as of the date of this news release,
and Biohaven does not undertake any obligation to update
any forward-looking statements, whether as a result of new
information, future events or otherwise, except as required by
law.
Investor Contact:
Jennifer
Porcelli
Vice President, Investor Relations
jennifer.porcelli@biohavenpharma.com
201-248-0741
Media Contact:
Mike
Beyer
Sam Brown Inc.
mikebeyer@sambrown.com
312-961-2502
MoDE is a trademark of Biohaven Therapeutics Ltd.
Biohaven AAN 2024 Oral & Poster
Presentations:
Functional Impairments in Patients with KCNQ2-DEE: Associations
Among Key Clinical Features
Sunday 4/14/24: 8:00-9:00
P1- Poster Session 1
Colorado Convention Center –
Exhibit Hall B-E
The Phase 3 RESILIENT Study: Taldefgrobep Alfa in Spinal
Muscular Atrophy
Sunday 4/14/24: 11:45 - 12:45
P2 - Poster Session 2
Colorado Convention Center -
Exhibit Hall
Association of Anti-inflammatory Therapy Use with the Incidence
of Parkinson's Disease: A Person-Time Analysis Among Patients with
Autoimmune Diseases
Sunday 4/14/24: 1:00-3:00 (1:24-1:36)
S2 – Movement Disorders: Epidemiology and Clinical Aspects
Colorado Convention Center-
Mile High 4CD
Re-weighting MDS-UPDRS Motor Items for Optimal Sensitivity to
Parkinson's Disease Progression in Untreated Patients Using
Parkinson's Progression Markers Initiative Data
Sunday 4/14/24: 1:00-3:00 (1:36-1:48)
S2 – Movement Disorders: Epidemiology and Clinical Aspects
Colorado Convention Center-
Mile High 4CD
Population Pharmacokinetic Modeling of Riluzole After
Administration of a Next Generation Prodrug Troriluzole
Sunday 4/14/24: 1:00 - 3:00 (2:12-2:24)
S3 - General Neurology 1
Colorado Convention Center - Four
Seasons 2/3
Next Generation Prodrug Troriluzole: Increased Bioavailability
of Riluzole with No Food Effect in Healthy Subjects
Sunday 4/14/24: 3:30 - 5:30 (4:30-4:42)
S5 - ALS and CMT: New Therapeutic Approaches
Colorado Convention Center - Four
Seasons 1
BHV-2100, A First-In-Class TRPM3 Antagonist for the Treatment of
Pain
Monday 4/15/24: 11:15-12:15 (11:27-11:39)
S13 – Pain Research
Colorado Convention Center 605
Troriluzole Exhibits Favorable Hepatic Safety Profile Across a
Diverse Range of Disorders
Monday 4/15/24: 11:45 - 12:45
P4 - Poster Session 4
Colorado Convention Center -
Exhibit Hall
Safety, Tolerability, and Pharmacokinetics of Single and
Multiple Rising Doses of a Next Generation Prodrug Troriluzole in
Healthy Subjects
Monday 4/15/24: 11:45 - 12:45
P4 - Poster Session 4
Colorado Convention Center -
Exhibit Hall
No Clinically Relevant Effects of Hepatic Impairment on the
Pharmacokinetics of a Next Generation Prodrug Troriluzole
Monday 4/15/24: 11:45 - 12:45
P4 - Poster Session
Colorado Convention Center -
Exhibit Hall
Automated Video-based Characterization of Movement Quality in a
Phase III Clinical Trial of Troriluzole in Subjects with
Spinocerebellar Ataxia
Tuesday 4/16/24: 8:00-9:00
P6- Poster Session 6
Colorado Convention Center –
Exhibit Hall
Psychometric Validation of the Modified-functional Scale for the
Assessment and Rating of Ataxias
Tuesday 4/16/24: 11:45-12:45
P7 – Poster Session 7
Colorado Convention Center –
Exhibit Hall
Development of a Novel Composite Measure (SCACOMS) to Assess
Disease Progression in Spinocerebellar Ataxia
Tuesday 4/16/24: 11:45-12:45
P7 - Poster Session 7
Colorado Convention Center –
Exhibit Hall
Phase 1 Study Evaluating the Safety and Tolerability of
BHV-7000, a Novel, Selective Kv7.2/7.3 Potassium Channel Activator,
in Healthy Adults
Tuesday 4/16/24: 5:30 - 6:30
P8 - Poster Session 8
Colorado Convention Center -
Exhibit Hall
Novel, Selective Kv7.2/7.3 Potassium Channel Activator,
BHV-7000, Demonstrates Dose-dependent Pharmacodynamic Effects on
EEG Parameters in Healthy Adults
Tuesday 4/16/24: 5:30 - 6:30
P8 - Poster Session 8
Colorado Convention Center -
Exhibit Hall
Determinants of Health-related Quality of Life of Patients with
Focal Epilepsy: A Systematic Literature Review
Wednesday 4/17/24: 8:00-9:00
P9- Poster Session 9
Colorado Convention Center –
Exhibit Hall
Characterization of BHV-7000: A Novel Kv7/2/7.3 Activator for
the Treatment of Seizures
Wednesday 4/17/24: 1:00-3:00 (2:00-2:12)
S29- Epilepsy Diagnostics and Therapeutics
Colorado Convention Center 605
Matching-adjusted Indirect Comparison of Troriluzole Versus
Untreated Natural History Cohort in Spinocerebellar Ataxia
Wednesday 4/17/24: 3:30-5:30 (5:06-5:18)
S35 – Movement Disorders: Hyperkinetic Movement Disorders
Colorado Convention Center – Four
Seasons 4
Re-weighting MDS-UPDRS Part II Items for Optimal Sensitivity to
Parkinson's Disease Progression Using Parkinson's Progression
Markers Initiative Natural History Data
Wednesday 4/17/24: 5:30-6:30
P11 – Poster Session 11
Colorado Convention Center –
Exhibit Hall
Novel Bispecific Degrader BHV-1300 Achieves Rapid, Robust, and
Selective IgG Reduction in Preclinical Models Including Nonhuman
Primates
Thursday 4/18/24: 1:00 - 3:00 (1:36-1:48)
S43 - General Neurology 2
Colorado Convention Center -
108/110/112
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SOURCE Biohaven Ltd.