Active Biotech completes safety evaluation in tasquinimod study
The first cohort finished the assessment, confirming tolerability for the revised regimen, and recruitment continues with three more patients.
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Biotechnology company developing treatments for cancer and inflammatory eye diseases
activebiotech.comLast updated
In short: Active Biotech completed tasquinimod safety cohort, secured Japan laquinimod patent, expanded US collaboration, and reported Q2 loss.
The first cohort finished the assessment, confirming tolerability for the revised regimen, and recruitment continues with three more patients.
Japan Patent Office granted patent covering laquinimod formulation for severe inflammatory eye diseases like non-infectious uveitis.
The collaboration aims to accelerate clinical development of tasquinimod for myelofibrosis. A preclinical program is launched to validate the drug's effect.
The Phase Ib/II study evaluates tasquinimod in myelofibrosis patients refractory to JAK2 inhibitors, with greater dosing flexibility.
Active Biotech AB (publ) (ACTI.ST), an immunomodulatory treatment company, on Thursday announced interim financial results for the second quarter and registered a marginally lower loss...
Lund Sweden, July 24, 2026 - Active Biotech (NASDAQ STOCKHOLM: ACTI) today announced that the first patient has been dosed in the Phase Ib/II clinical...
The Annual General Meeting in Active Biotech AB (publ) ("Active Biotech" or the "Company") held on May 20, 2026, resolved to carry out a reverse...
LONDON and PHILADELPHIA, May 19, 2026 (GLOBE NEWSWIRE) -- Avacta Therapeutics (AIM: AVCT, “the Company”, “Avacta”), a clinical stage biopharmaceutical company developing pre|CISION, a tumor-activated...
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