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Systematic, data-driven science coverage · Monday, October 12, 2026
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Mirum's brelovitug aces Phase III in chronic hepatitis delta virus with 56% response rate
Development

Mirum's brelovitug aces Phase III in chronic hepatitis delta virus with 56% response rate

Mirum Pharmaceuticals (Nasdaq: MIRM) reported that the Phase III portion of the AZURE-1 study of brelovitug, an anti-hepatitis B surface antigen (HBsAg)...

5d ago
ADARx raises USD 446m in upsized Nasdaq IPO
Business

ADARx raises USD 446m in upsized Nasdaq IPO

San Diego-based ADARx Pharmaceuticals priced an upsized initial public offering of 26.25 million shares at USD 17 per share, raising approximately USD 446.3...

5d ago
Carvykti sustains five-year remissions in half of early-line relapsed myeloma patients
Development

Carvykti sustains five-year remissions in half of early-line relapsed myeloma patients

Johnson & Johnson (NYSE: JNJ) reported five-year follow-up data from the Phase II CARTITUDE-2 study showing that half of patients with early-line relapsed...

5d ago
Roche taps Atavistik Bio in USD 1.9bn allosteric drug discovery deal
Business

Roche taps Atavistik Bio in USD 1.9bn allosteric drug discovery deal

Cambridge, Massachusetts-based Atavistik Bio entered a strategic research collaboration with Roche (OTCQX: RHHBY) to discover small-molecule therapies...

5d ago
Tolerance Bio adds to thymus pipeline with anti-IL-33 antibody license from Tanabe
Business

Tolerance Bio adds to thymus pipeline with anti-IL-33 antibody license from Tanabe

Philadelphia-based Tolerance Bio, Inc. has licensed TLB-33 (MT-2990), a clinical-stage anti-IL-33 monoclonal antibody, from Japan-based Tanabe Pharma...

5d ago
Merck strikes USD 2.13bn deal for China-origin preclinical KRAS G12D inhibitor
Business

Merck strikes USD 2.13bn deal for China-origin preclinical KRAS G12D inhibitor

Merck (NYSE: MRK) has agreed to pay USD 400 million upfront to exclusively license SPR2015, a preclinical oral KRAS G12D-targeted RAS(ON) inhibitor from...

5d ago
AstraZeneca wins Priority Review for Imfinzi-EV regimen in bladder cancer
Regulatory & Policy

AstraZeneca wins Priority Review for Imfinzi-EV regimen in bladder cancer

The US FDA granted Priority Review to AstraZeneca’s supplemental BLA for perioperative Imfinzi (durvalumab) with neoadjuvant enfortumab vedotin...

5d ago
AbbVie lands FDA approval for Cerevel-origin Parkinson’s drug Juvmo
Regulatory & Policy

AbbVie lands FDA approval for Cerevel-origin Parkinson’s drug Juvmo

AbbVie (NYSE: ABBV) received US FDA approval for Juvmo (tavapadon) for the treatment of Parkinson's disease in adults, with the drug approved for use with...

5d ago
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UMass Chan, Mass General Brigham advance first gene therapy trial in mucolipidosis type IV
Regulatory & Policy

UMass Chan, Mass General Brigham advance first gene therapy trial in mucolipidosis type IV

The US FDA has allowed an investigational new drug (IND) application to proceed for AAV-MCOLN1, an adeno-associated virus gene therapy for mucolipidosis...

5d ago
Finland's Kasvu secures EUR 30m Series A for non-hallucinogenic depression drug
Business

Finland's Kasvu secures EUR 30m Series A for non-hallucinogenic depression drug

Finland-based Kasvu Therapeutics has raised EUR 30 million (USD 34.4 million) in a Series A financing to advance KTX-0141, a small-molecule TrkB positive...

Sep 28
Incyte/Mirum take FDA approval for Atebrioz as first oral ALK2i for fibrodysplasia ossificans progressiva
Regulatory & Policy

Incyte/Mirum take FDA approval for Atebrioz as first oral ALK2i for fibrodysplasia ossificans progressiva

The US FDA approved Atebrioz (zilurgisertib), an oral ALK2 inhibitor developed by Incyte (Nasdaq: INCY) and commercialized by Mirum Pharmaceuticals (Nasdaq:...

5d ago
FDA keeps Newron’s ENIGMA-TRS 2 study on clinical hold
Development

FDA keeps Newron’s ENIGMA-TRS 2 study on clinical hold

Italy-based Newron Pharmaceuticals (SIX: NWRN, XETRA: NP5) said the US FDA’s clinical hold on new patient enrollment at US sites in the Phase III ENIGMA-TRS...

Sep 28
nChroma Bio's epigenetic silencer therapy shows sustained HBV suppression in preclinical models
Discovery

nChroma Bio's epigenetic silencer therapy shows sustained HBV suppression in preclinical models

Researchers at Boston-based genetic medicines company nChroma Bio published preclinical data in Nature Biomedical Engineering supporting CRMA-1001, an...

5d ago
Prime Medicine receives FDA clearance for PM647 in alpha-1 antitrypsin deficiency
Regulatory & Policy

Prime Medicine receives FDA clearance for PM647 in alpha-1 antitrypsin deficiency

Cambridge, Massachusetts-based Prime Medicine, Inc. (Nasdaq: PRME) received US FDA clearance to begin first-in-human testing of PM647, a one-time in vivo...

5d ago
Amplifyer Bio humanized priming agent boosts ctDNA recovery up to 100-fold in mice
Discovery

Amplifyer Bio humanized priming agent boosts ctDNA recovery up to 100-fold in mice

Amplifyer Bio, an MIT and Broad Institute spinout developing agents designed to increase the amount of circulating tumor DNA (ctDNA) recoverable from blood,...

Sep 28