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Bluebird bio

Dec 15, 2023

Lyfgenia or Casgevy: Who Will Lead the Sickle Cell Disease Treatment Space?

Dec 12, 2023

Merck and Moderna Initiate Study to Evaluate V940; FDA Approves Vertex and CRISPR Therapeutics’ CASGEVY for SCD; Novartis Updated on its Investigational Iptacopan Phase III Study; FDA Grants Priority Review for New Drug Application for Elafibranor; FDA Approves bluebird bio’s LYFGENIA for Patients SCD; FDA Fast Track Designation for DMD Gene Therapy

May 12, 2023

Gene Therapy in Rare Disorders: Acceptance in Europe Faces Challenges

Apr 25, 2023

Janssen’s AKEEGA Approval; FDA Approves Roche’s Polivy Combo for Frontline B-cell Lymphoma; Daiichi Sankyo’s Quizartinib for Adults With FLT3-ITD-Positive AML; bluebird bio BLA for lovo-cel for Patients with Sickle Cell Disease; Fast Track Designation for Lu-PNT2002 for mCRPC Treatment; FDA Orphan Drug Designation to XORTX’s Oxypurinol

Apr 14, 2023

Vertex/CRISPR’s Gene-editing Therapy exa-cel: Inch Ahead of Rival

Jan 12, 2021

Birinapant licensing; AvantGen, IGM pairs up for anti-SARS-CoV-2 antibodies; BeiGene, Novartis to co-dvelop Tislelizumab; Valo raises USD190 M; Bluebird Bio Spins-off

Jul 31, 2020

A Complex Chromosomal Abberation Called Adrenoleukodystrophy

May 08, 2020

Overcoming the prevailing unmet needs in Beta-Thalassemia Market

Feb 18, 2020

Why should every company working on CAR-T therapy attend CAR TCR Summit Europe?

Nov 25, 2019

How Gene therapy is changing the Beta-thalassemia Treatment outlook?

Newsletter/Whitepaper