News about "Biopharmaceutical Innovation"

Argo Biopharma Doses First Patient in Phase 1 siRNA Trial

Argo Biopharma Doses First Patient in Phase 1 siRNA Trial

Argo Biopharma has dosed the first participant in the phase I trial of BW-41012, its Factor XI-targeting siRNA therapy for preventing thromboembolic diseases.

Biopharmaceutical Innovation | 22/07/2026 | By News Bureau 137

India Poised to Become a Global Biopharma Leader: Anupriya Patel

India Poised to Become a Global Biopharma Leader: Anupriya Patel

Union Minister Anupriya Patel said India is well-positioned to become a global biopharma leader, highlighting the Biopharma SHAKTI initiative’s goal of launching 100 biologics by 2047. She urged the industry to strengthen capabilities in biologics and biosimilars.

Biopharmaceutical Innovation | 12/06/2026 | By News Bureau 137

Travere Therapeutics Receives USPTO Patent Allowance for Filspari Use in IgA Nephropathy

Travere Therapeutics Receives USPTO Patent Allowance for Filspari Use in IgA Nephropathy

Travere Therapeutics has secured a Notice of Allowance from the USPTO for a patent application covering specific methods of using Filspari (sparsentan) in the treatment of IgA nephropathy, strengthening its rare kidney disease portfolio.

Biopharmaceutical Innovation | 29/05/2026 | By News Bureau 203

Pharming Secures EU Approval for Joenja as First Targeted Treatment for Rare Immune Disorder APDS

Pharming Secures EU Approval for Joenja as First Targeted Treatment for Rare Immune Disorder APDS

Pharming Group has received European Commission approval for Joenja, expanding treatment access for patients with activated PI3K delta syndrome and strengthening therapeutic options for rare immune disorders.

Biopharmaceutical Innovation | 26/05/2026 | By News Bureau 104

Incyte and Genesis Molecular AI Expand Strategic Collaboration to Accelerate AI-Driven Drug Discovery

Incyte and Genesis Molecular AI Expand Strategic Collaboration to Accelerate AI-Driven Drug Discovery

Incyte and Genesis Molecular AI have expanded their strategic collaboration to deploy advanced molecular AI technologies and proprietary research data, aiming to accelerate drug discovery and develop next-generation therapies through AI-powered molecular design.

Biopharmaceutical Innovation | 22/05/2026 | By News Bureau 286

Alebund Pharmaceuticals Completes Enrollment in Global Phase 3 Trial for AP301 Hyperphosphatemia Therapy

Alebund Pharmaceuticals Completes Enrollment in Global Phase 3 Trial for AP301 Hyperphosphatemia Therapy

Alebund Pharmaceuticals has completed patient enrollment in its global phase 3 RESPOND-2 study evaluating AP301, a next-generation phosphate binder for CKD patients on dialysis.

Biopharmaceutical Innovation | 07/05/2026 | By News Bureau 163

GSK's Efimosfermin Secures FDA Breakthrough and EMA PRIME Status for MASH Treatment

GSK's Efimosfermin Secures FDA Breakthrough and EMA PRIME Status for MASH Treatment

The dual regulatory designations from US FDA and European Medicines Agency fast-track development of GSK’s investigational liver therapy for metabolic dysfunction-associated steatohepatitis.

Biopharmaceutical Innovation | 29/04/2026 | By News Bureau 196

ImmunoForge Unveils LMT15 Platform to Transform CNS Drug Delivery

ImmunoForge Unveils LMT15 Platform to Transform CNS Drug Delivery

The clinical-stage biotech firm ImmunoForge is advancing its next-generation blood-brain barrier shuttle technology, combining enhanced brain permeability with long-acting formulations to accelerate therapies for CNS and rare diseases.

Biopharmaceutical Innovation | 24/04/2026 | By News Bureau 127

Abbisko's Irpagratinib Secures EMA Orphan Drug Tag for Liver Cancer

Abbisko's Irpagratinib Secures EMA Orphan Drug Tag for Liver Cancer

European regulator grants rare disease designation to FGFR4 inhibitor, boosting its clinical development and commercial prospects in hepatocellular carcinoma.

Biopharmaceutical Innovation | 01/04/2026 | By News Bureau 153

EU Grants Conditional Approval to Rezurock for Chronic GVHD Treatment

EU Grants Conditional Approval to Rezurock for Chronic GVHD Treatment

European Commission authorises belumosudil for patients aged 12 plus with limited treatment options, marking a significant advance in managing a life-threatening post-transplant condition.

Biopharmaceutical Innovation | 01/04/2026 | By News Bureau 117


 

 

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