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BioWorld - Saturday, December 27, 2025
Home » Topics » Immune, BioWorld

Immune, BioWorld
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Takeda shares findings from phase III study for post-op antiviral treatment maribavir

June 11, 2021
By Gina Lee
Takeda Pharmaceutical Co. Ltd. said findings from its phase III Solstice study testing oral antiviral TAK-620 (maribavir) in treating solid organ transplant recipients with cytomegalovirus infections resistant or refractory to prior therapy (R/R CMV), showed twice the rate of confirmed CMV viremia clearance compared to other conventional therapies.
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EHA 2021: Sanofi plots H2 refile for CAD drug sutimlimab after announcing further phase III data

June 11, 2021
By Richard Staines
Sanofi SA has announced new pivotal data that will form the basis of a refiling of rare disease drug sutimlimab for people with cold agglutinin disease (CAD).
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Novartis closes in on label expansion for Cosentyx after psoriasis win

June 2, 2021
By Richard Staines
Novartis AG is closing in on a label expansion for its blockbuster inflammatory disease drug, Cosentyx (secukinumab), after announcing supportive phase III results in children with two subtypes of juvenile idiopathic arthritis (JIA).
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Pill in immersive interface

Exscientia and BMS expand AI drug discovery deal, with potential $1.2B+ value

May 19, 2021
By Michael Fitzhugh
Building on a deal first struck in 2019, artificial intelligence (AI) specialist Exscientia Ltd. has agreed to take responsibility for a multitarget drug discovery collaboration with Bristol Myers Squibb Co. that could be worth more than $1.2 billion in all. The expanded collaboration, first established with BMS-acquired Celgene Corp., includes $50 million in up-front funding, up to $125 million in near to mid-term potential milestones, plus additional clinical, regulatory and commercial payments. It remains focused on small-molecule drug candidates in areas including oncology and immunology.
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N. brasiliensis

AAI 2021: In immunity, IL-33 signals stop as well as go

May 12, 2021
By Anette Breindl
Parasitic worms, or helminths, are a major global health issue. At the same time, "parasites have been a prolific area of biomedical research to emerge," De'Broski Herbert told his audience at the 2021 annual meeting of the American Association of Immunologists.
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RNA strand

Sanofi buys mRNA-focused Tidal Therapeutics in $470M deal

April 12, 2021
By Michael Fitzhugh
In a move that Sanofi SA said will bring it an mRNA-based research platform with applications in oncology, immunology and other diseases, the company has acquired Tidal Therapeutics Inc. for $160 million up front and up to $310 million in milestone payments. The preclinical startup, led by Merrimack Pharmaceuticals Inc. and Torque Therapeutics Inc. co-founder Ulrik Nielsen, is based in Cambridge, Mass.
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Red rocket launch button on keyboard
Newco news

U.S.-China cross-border biopharma launched to target autoimmune diseases

March 26, 2021
By Sergio Held
Zenas Biopharma LLC launched on March 23 as a U.S. funded cross-border biotech company targeting autoimmune diseases in China. The company, headquartered in Miromar Lakes, Fla., is founded and funded by Tellus Bioventures LLC and Fairmount Funds Management LLC.
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Savara goes back for seconds; inhaled fix for aPAP at last?

March 22, 2021
By Randy Osborne
As the firm doubles down on a therapy for the rare and terrible lung disease called autoimmune pulmonary alveolar proteinosis (aPAP), Savara Inc. met with little trouble raising money, disclosing March 15 a public offering that grossed $130 million.
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Multiple sclerosis

Can ya, Gilenya? J&J’s Ponvory for MS aims to intervene in sphingosine

March 19, 2021
By Randy Osborne
Now that Johnson & Johnson (J&J), through its Janssen Pharmaceuticals unit, has won the FDA’s nod for Ponvory (ponesimod), market factors will decide how the once-daily oral selective sphingosine-1-phosphate receptor 1 modulator fares against several others already approved in the class.
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Green approved stamp

Remegen wins China approval for lupus drug telitacicept

March 12, 2021
By Elise Mak
Remegen Co. Ltd.’s RC-18 (telitacicept) was granted conditional approval for systemic lupus erythematosus (SLE), marking the first NDA approval for the company that launched the world’s biggest biotech IPO last year.
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