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Intellectia

BRNS News

Investor Rights Law Firm Investigates Multiple Companies for Potential Violations

Mar 16 2026PRnewswire

Barinthus Biotherapeutics Financial Report Analysis

Mar 13 2026seekingalpha

Barinthus Biotherapeutics PLC Sponsored ADR (BRNS) Receives Upgrade to Buy: Implications for the Stock

Dec 15 2025NASDAQ.COM

Barinthus Bio Reports Positive Progress in Celiac Disease Immunotherapy Trial

Dec 10 2025Newsfilter

Halper Sadeh LLC Urges HFWA, BRNS, FITB Shareholders to Reach Out for Rights Consultation

Nov 20 2025Globenewswire

Halper Sadeh LLC Encourages BRNS, FITB, ADVM, HBAN Shareholders to Contact the Firm to Discuss Their Rights

Nov 19 2025PRnewswire

Halper Sadeh LLC Urges Shareholders of HFWA, FITB, AVDL, and BRNS to Reach Out for Rights Consultation

Nov 18 2025Globenewswire

$HAREHOLDER ALERT: M&A Class Action Firm Ongoing Investigation into Mergers Involving CMA, HFWA, BRNS, and FITB

Nov 18 2025Globenewswire

BRNS Events

03/13 08:10
Barinthus Bio and Clywedog Merger Outlook Positive
"As we move into 2026, we are excited by the proposed combination of Barinthus Bio and Clywedog, which positions us for multiple near-term catalysts emerging from our differentiated and complimentary clinical portfolio." said Bill Enright, Chief Executive Officer of Barinthus Bio. "We finished 2025 reporting encouraging results from the single ascending dose portion of the Phase 1 AVALON clinical trial of VTP-1000 in celiac disease, and expect multiple ascending dose data in the second half of 2026. These upcoming results will help us confirm whether VTP-1000 has the potential to be disease-modifying by restoring balance to the immune system."
12/10 08:20
Barinthus Biotherapeutics Updates on VTP-1000 Phase 1 Trial Progress
Barinthus Biotherapeutics announced an update on its first-in-human Phase 1 trial of VTP-1000 in adults with celiac disease. In the single ascending dose, SAD, portion of the trial, VTP-1000 was well tolerated with no treatment-related serious adverse events, SAEs, and a dose-dependent pharmacological effect observed. The multiple ascending dose, MAD, portion of the trial, which includes a gluten challenge, is ongoing with data expected in the second half of 2026. The SAD portion of the Phase 1 AVALON trial enrolled 18 patients in three placebo-controlled cohorts of ascending doses. VTP-1000 was well tolerated at all dose levels with no treatment-related SAEs. Pharmacological data collected showed a dose-dependent effect.
11/07 07:33
Barinthus Biotherapeutics announces Q3 earnings per share of 36 cents, compared to a loss of 21 cents in the same period last year.
"The proposed combination of Barinthus Bio and Clywedog represents an important step toward building a stronger, more resilient company, with several expected near-term catalysts." said Bill Enright, Chief Executive Officer of Barinthus Bio. "By combining our complementary pipelines and deep expertise in metabolic and autoimmune diseases, we are diversifying risk across multiple assets and creating a differentiated portfolio. This combination will position us to advance disease-modifying therapies for Type 1 and Type 2 diabetes, celiac disease, and other serious conditions."

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