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Bright Minds to Announce Topline Results for BMB-101 Phase 2 Trial in Absence Seizures and Developmental and Epileptic Encephalopathies on Tuesday, January 6, 2026

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earnings date clinical trial

Bright Minds Biosciences (NASDAQ:DRUG) will report topline Phase 2 results for BMB-101 on January 6, 2026 at 8:00 AM ET. The company said the announcement covers patients with drug-resistant absence seizures and developmental and epileptic encephalopathy.

A live conference call and webcast will present the data, include a discussion and a Q&A session, and a replay will be posted in the company’s Investors > Events and Presentations section after the event. Participants can submit questions using the webcast "Questions" tab.

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News Market Reaction 23 Alerts

-4.13% News Effect
+63.2% Peak Tracked
-9.6% Trough Tracked
-$27M Valuation Impact
$623M Market Cap
1.5x Rel. Volume

On the day this news was published, DRUG declined 4.13%, reflecting a moderate negative market reaction. Argus tracked a peak move of +63.2% during that session. Argus tracked a trough of -9.6% from its starting point during tracking. Our momentum scanner triggered 23 alerts that day, indicating elevated trading interest and price volatility. This price movement removed approximately $27M from the company's valuation, bringing the market cap to $623M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

NOVA trial duration 16 weeks Phase 2a NOVA study of BMB-101 in Prader-Willi syndrome
NOVA extension 9 months Optional open-label extension for NOVA Phase 2a study
Male efficacy 1h 86% vs 81% BMB-201 vs sumatriptan in male rats at 1 hour
Male efficacy 2h 53–64% vs 44% BMB-201 vs sumatriptan in male rats at 2 hours
Female efficacy 1h 76–100% vs 56% BMB-201 vs sumatriptan in female rats at 1 hour
Female efficacy 2h 80% vs 63% BMB-201 vs sumatriptan in female rats at 2 hours
Janus Henderson stake 1,145,660 shares (16.3%) Schedule 13G/A filing dated Aug 14, 2025
Sio Capital stake 512,338 shares (7.27%) Schedule 13G/A filing dated Aug 13, 2025

Market Reality Check

$86.75 Last Close
Volume Volume 253,686 is 44% above average (176,179), indicating elevated pre-event interest. normal
Technical Price 80.01 is trading above the 200-day MA of 45.12, reflecting a sustained uptrend ahead of results.

Peers on Argus

DRUG gained 6.95% while close biotech peers like LRMR (-3.72%), ASMB (-4.15%), IMRX (-2.51%), MBX (-4.71%), and TECX (-0.33%) declined, pointing to a stock-specific move tied to the upcoming topline data.

Historical Context

Date Event Sentiment Move Catalyst
Nov 25 Conference appearances Positive +1.0% Highlighted 5-HT2 agonist work at major December 2025 healthcare and epilepsy meetings.
Nov 17 Advisory board expansion Positive +0.2% Added PWS experts to advisory board supporting BMB-101 and BMB-105 development.
Nov 06 Program initiation Positive +7.5% Launched PWS program, NOVA Phase 2a BMB-101 study, and BMB-105 Phase 1 plans.
Oct 30 Conference and options Positive +0.5% Outlined November 2025 conference talks and granted director and officer stock options.
Sep 04 Preclinical results Positive +1.6% Reported BMB-201 outperformed sumatriptan in a validated preclinical headache model.
Pattern Detected

Recent pipeline and event-driven announcements have typically produced modest positive price reactions, with a stronger move following the November 2025 PWS program update.

Recent Company History

Over the last six months, Bright Minds has advanced multiple CNS programs and increased visibility through conferences and advisory board expansions. Notable events include initiating the PWS program and Phase 2a NOVA study, plus highlighting BMB-201’s preclinical efficacy in vascular headache models. These updates saw generally positive one-day moves up to 7.55%. Today’s announcement of a firm January 6, 2026 topline readout date fits the pattern of clinically focused, data-driven catalysts.

Market Pulse Summary

This announcement sets a firm January 6, 2026 date for Phase 2 topline data from BMB-101 in drug-resistant absence seizures and developmental and epileptic encephalopathies, framing a clear clinical catalyst. Recent history shows steady progress across epilepsy, PWS, and vascular headache programs with generally positive single-day reactions. Investors may focus on seizure-control efficacy, safety outcomes, and how BMB-101 results influence the broader 5-HT–targeted CNS pipeline.

Key Terms

phase 2 medical
"to report topline results for the Phase 2 trial of BMB-101 in patients"
Phase 2 is the mid-stage clinical trial where a new drug or treatment is tested in a larger group of patients to see if it works and to keep checking safety after initial human testing. Think of it as a field test that proves whether a product actually delivers its promised benefit. Investors watch Phase 2 closely because its results strongly influence a medicine’s chances of reaching the market, the size of its potential sales, and the company’s valuation.
developmental and epileptic encephalopathy medical
"drug-resistant Absence Seizures and Developmental and Epileptic Encephalopathy."
A severe neurological condition that begins in infancy or early childhood, marked by frequent, hard-to-control seizures and slowing or loss of normal development such as movement, learning and communication. Think of it as a critical control system in a child’s brain that malfunctions and interferes with growth and daily function. For investors it signals a high unmet medical need, focused regulatory attention and the potential for significant commercial value — but also greater clinical and development risk for therapies.
5-ht receptor agonists medical
"developing highly selective 5-HT receptor agonists for neurological and psychiatric disorders"
5-HT receptor agonists are drugs that bind to and activate specific serotonin receptors in the brain and body, essentially turning on signals that serotonin normally controls. Like flipping a particular light switch to change how a room behaves, these medicines can alter mood, pain perception, digestion or blood vessel tone; investors track them because clinical trial results, regulatory approvals and market demand directly affect a drug developer’s revenue prospects and stock value.

AI-generated analysis. Not financial advice.

– Conference Call and Live Webcast at 8AM ET –

NEW YORK, Jan. 05, 2026 (GLOBE NEWSWIRE) -- Bright Minds Biosciences Inc. (CSE: DRUG) (Nasdaq: DRUG) (“Bright Minds” or the “Company”), a clinical-stage biotechnology company focused on developing highly selective 5-HT receptor agonists for neurological and psychiatric disorders, today announced that it will host a conference call and live webcast at 8:00AM ET on January 6, 2026, to report topline results for the Phase 2 trial of BMB-101 in patients with drug-resistant Absence Seizures and Developmental and Epileptic Encephalopathy.

Webcast Information

The Bright Minds virtual event will be webcast live and a replay will be available after the event by visiting the “Investors” section of the Company’s website and selecting “Events and Presentations.”

Date and Time: January 6, 2026, 8AM ET
Webcast: https://app.livestorm.co/bright-minds-biosciences/bmb-101-topline-data-announcement

The call will include a discussion of the data followed by a Q&A session. Individuals who wish to ask questions should use the “Questions” tab available during the live webcast.​

About Bright Minds Biosciences
Bright Minds is a biotechnology company developing innovative treatments for patients with neurological and psychiatric disorders. Our pipeline includes novel compounds targeting key receptors in the brain to address conditions with high unmet medical need, including Rare Epilepsy, Prader-Willi Syndrome, Depression, and other CNS disorders. Bright Minds is focused on delivering breakthrough therapies that can transform patients' lives.

Bright Minds has developed a unique platform of highly selective serotonergic agonists exhibiting selectivity at different serotonergic receptors. This has provided a rich portfolio of NCE programs within neurology and psychiatry.​

Contact
Alex Vasilkevich
Chief Operating Officer
Bright Minds Biosciences Inc.
T: 414-731-6422
E: alex@brightmindsbio.com

Investor Relations
Lisa M. Wilson
T: 212-452-2793
E: lwilson@investorrelations.com


FAQ

When will Bright Minds (DRUG) release BMB-101 Phase 2 topline results?

Topline results will be announced on January 6, 2026 at 8:00 AM ET.

What conditions are included in the BMB-101 Phase 2 announcement for DRUG?

The announcement covers drug-resistant absence seizures and developmental and epileptic encephalopathy.

How can investors join the Bright Minds (DRUG) webcast for the BMB-101 topline data?

Join the live webcast via the provided link at 8:00 AM ET on January 6, 2026 and use the "Questions" tab to ask questions.

Will Bright Minds (DRUG) make a replay of the BMB-101 presentation available?

Yes. A replay will be available after the event in the company’s Investors > Events and Presentations section.

Will the BMB-101 webcast include a Q&A session for analysts and investors?

Yes. The call will include a discussion of the data followed by a Q&A session where participants can ask questions via the webcast.

Where is the Bright Minds (DRUG) BMB-101 webcast hosted online?

The webcast is hosted at the company’s livestream page: https://app.livestorm.co/bright-minds-biosciences/bmb-101-topline-data-announcement.
Bright Minds Biosciences Inc

NASDAQ:DRUG

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Biotechnology
Healthcare
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United States
New York