IPP Bureau

EU to withdraw Levamisole medicines over risk of rare, deadly brain disorder
EU to withdraw Levamisole medicines over risk of rare, deadly brain disorder

By IPP Bureau - February 17, 2026

The recommendation is based on new data from continuous safety monitoring of medicines in the EU

Irish medtech firm InVera Medical wins EU nod for breakthrough vein treatment device
Irish medtech firm InVera Medical wins EU nod for breakthrough vein treatment device

By IPP Bureau - February 17, 2026

Teva and Sanofi duvakitug Phase 2b data show sustained efficacy in IBD
Teva and Sanofi duvakitug Phase 2b data show sustained efficacy in IBD

By IPP Bureau - February 17, 2026

Duvakitug was well tolerated and safety was consistent with the induction study

Moderna’s new Covid vaccine mNEXSPIKE wins European approval
Moderna’s new Covid vaccine mNEXSPIKE wins European approval

By IPP Bureau - February 17, 2026

mNEXSPIKE is the third Moderna vaccine authorized in the European Union, strengthening the Company's respiratory vaccine portfolio in Europe

FDA grants priority review to Bristol Myers Squibb's Iberdomide for multiple myeloma
FDA grants priority review to Bristol Myers Squibb's Iberdomide for multiple myeloma

By IPP Bureau - February 17, 2026

Iberdomide has the potential to be the first approved CELMoD agent

Roche appoints Mark Dawson as new Head of Pharma Research and Early Development
Roche appoints Mark Dawson as new Head of Pharma Research and Early Development

By IPP Bureau - February 17, 2026

Dawson joins Roche from the Peter MacCallum Cancer Centre, where he serves as Associate Director of Research

Indian pharma market grew 10.2% yoy in January 2026
Indian pharma market grew 10.2% yoy in January 2026

By IPP Bureau - February 17, 2026

Ind-Ra expects chronic therapies to outpace IPM as compliance improves and lifestyle diseases rise

Biofrontera scores FDA filing acceptance for Ameluz PDT in skin cancer breakthrough
Biofrontera scores FDA filing acceptance for Ameluz PDT in skin cancer breakthrough

By IPP Bureau - February 16, 2026

If approved, Ameluz would become the first and only photodynamic therapy (PDT) photosensitizer for sBCC in the US

Dewpoint Therapeutics selects groundbreaking MYC development candidate
Dewpoint Therapeutics selects groundbreaking MYC development candidate

By IPP Bureau - February 16, 2026

MYC, a master regulator of oncogenic transcription, drives multiple high-burden cancers but has long eluded direct pharmacologic control

STADA & Bio-Thera bag European nod for Gotenfia
STADA & Bio-Thera bag European nod for Gotenfia

By IPP Bureau - February 16, 2026

Clinigen bags Japan's nod to human milk-based medicine for preterm infants
Clinigen bags Japan's nod to human milk-based medicine for preterm infants

By IPP Bureau - February 16, 2026

PreemieFort Enteral Solution's approval marks the first time a nutritional product derived from human milk has been recognized as a prescription medicine anywhere in the world

Amgen scores EU nod for UPLIZNA in rare autoimmune disease
Amgen scores EU nod for UPLIZNA in rare autoimmune disease

By IPP Bureau - February 16, 2026

The approval marks a major advance in targeted treatment for this rare, chronic autoimmune disease, offering twice-yearly maintenance dosing after two initial loading doses

Lundbeck’s bocunebart shows breakthrough potential in migraine prevention
Lundbeck’s bocunebart shows breakthrough potential in migraine prevention

By IPP Bureau - February 16, 2026

Bocunebart works by blocking pituitary adenylate cyclase-activating polypeptide

BridgeBio reports breakthrough results in Phase 3 achondroplasia trial
BridgeBio reports breakthrough results in Phase 3 achondroplasia trial

By IPP Bureau - February 16, 2026

Achondroplasia is a genetic condition driven by FGFR3 that affects more than stature alone

Lyell Immunopharma launches groundbreaking Phase 3 CAR T-Cell trial for aggressive lymphoma
Lyell Immunopharma launches groundbreaking Phase 3 CAR T-Cell trial for aggressive lymphoma

By IPP Bureau - February 16, 2026

PiNACLE is a head-to-head study comparing its next-generation CAR T-cell therapy against established therapies liso-cel and axi-cel in patients with relapsed or refractory large B-cell lymphoma

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