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Home»Posts tagged with»rare disease therapeutics

Aisa Pharma’s AISA-021 shows mixed but promising signals in systemic sclerosis-associated Raynaud’s phenomenon

By Pallavi Madhiraju on March 8, 2026   Pharma & Biotech  

Aisa Pharma’s AISA-021 shows mixed but promising signals in systemic sclerosis-associated Raynaud’s phenomenon

Aisa Pharma’s AISA-021 shows promising Phase 2 signals in systemic sclerosis Raynaud’s. Discover what the RECONNOITER data could mean for future treatment.

Rallybio validates durable complement suppression with RLYB116 in Phase 1 study

By Pallavi Madhiraju on February 18, 2026   Pharma & Biotech  

Rallybio validates durable complement suppression with RLYB116 in Phase 1 study

Rallybio reports Phase 1 data for RLYB116 showing sustained complement inhibition. Find out what this changes for C5 therapies and what comes next.

Why BioCryst’s Astria acquisition reshapes long-acting competition in hereditary angioedema prophylaxis

By Soujanya Ravi on January 26, 2026   Pharma & Biotech  

Why BioCryst’s Astria acquisition reshapes long-acting competition in hereditary angioedema prophylaxis

BioCryst completes its Astria acquisition to expand long-acting hereditary angioedema leadership. Find out what this means for HAE treatment competition.

What does Swissmedic approval of Santhera’s AGAMREE mean for long-term steroid treatment in Duchenne muscular dystrophy?

By Soujanya Ravi on January 15, 2026   Pharma & Biotech  

What does Swissmedic approval of Santhera’s AGAMREE mean for long-term steroid treatment in Duchenne muscular dystrophy?

Swissmedic approves Santhera’s AGAMREE for Duchenne muscular dystrophy. Find out how vamorolone could reshape long-term steroid treatment strategies.

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