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BioWorld - Monday, March 9, 2026
Home » Topics » Disease categories and therapies » Hematologic

Hematologic
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Red blood cells

Protagonist’s rare blood disorder treatment whipsawed by an FDA rarity

April 14, 2022
By Lee Landenberger
It’s been one thing after another for rusfertide from Protagonist Therapeutics Inc. for the past year. Now the U.S. FDA has told the company it wants to rescind the breakthrough designation, a relatively rare occurrence, based on observed malignancies in a follow-up to September’s clinical hold.
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Stock market illustration

Sierra Oncology shares climb nearly 39% as GSK tables $1.9B offer

April 13, 2022
By Cormac Sheridan
Shares in Sierra Oncology Inc. (NASDAQ:SRRA) surged 38.5% to $54.75 on April 13 as Glaxosmithkline plc made a $55-per-share offer for the company, which values it at $1.9 billion. The offer represents a premium of about 39% on Sierra’s April 12 closing share price of $39.52 and a premium of about 63% over its volume-weighted average share price over the last 30 trading days.
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Zhejiang Hisun Pharmaceutical, Hisun Accuray Therapeutics patent anticoagulants

April 12, 2022

Third sacker: Bluebird plots major-league layoffs to stay in gene therapy game

April 5, 2022
By Randy Osborne
Bluebird Bio Inc. became the latest in a spate of gene therapy firms to disclose restructuring plans, as the company aims to save $160 million over the next two years, saying goodbye to about a third of its workforce. It’s the other shoe to drop after Cambridge, Mass.-based Bluebird rattled Wall Street with phraseology in the firm’s fourth-quarter earnings report March 4 that expressed “substantial doubt” regarding whether operations could go on.
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New NFE2-related factor 2 activators described by Sanofi

April 1, 2022

Filings ahead in hemophilia A: Sanofi, Sobi hit endpoints with once-weekly factor VIII drug

March 9, 2022
By Jennifer Boggs
Partners Sanofi SA and Swedish Orphan Biovitrum AB (Sobi) said regulatory submissions are expected this year for once-weekly factor VIII therapy efanesoctocog alfa in hemophilia A following top-line success in a pivotal phase III study, which showed a clinically meaningful prevention of bleeds in people with severe disease receiving prophylaxis over 52 weeks. The drug, also known as BIVV-001, has fast track and orphan designations in the U.S., and the companies are banking on its extended half-life to go up against blockbuster bispecific antibody Hemlibra (emicizumab) from Roche Holding AG as well as a potential gene therapy from Biomarin Pharmaceutical Inc.
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Procoagulant nanoparticles as platelet surrogates for management of bleeding

March 4, 2022

China Hinye Pharmaceutical presents prodrugs of the active metabolite of clopidogrel

Feb. 28, 2022

Microlyse targets VWF and clears microvascular thrombosis

Feb. 23, 2022
Hand holding dollar sign

Targed draws €39M series A to advance anti-thrombosis programs

Feb. 22, 2022
By Nuala Moran
LONDON – Targed Biopharmaceuticals BV has raised €39 million (US$44.2 million) in a series A financing that will enable it to take its targeted clot busting drug Microlyse into clinical development. The first-in-class product consists of urokinase, a serine protease involved in the conversion of inactive plasminogen to active plasmin, linked to a nanobody targeted at von Willebrand factor, the blood glycoprotein that plays a key role in hemostasis.
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