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BioWorld - Friday, January 2, 2026
Home » Novartis AG

Articles Tagged with ''Novartis AG''

Businesspeople shaking hands, meeting with cityscape, charts

Flare and Schrödinger join multibillion-dollar collaborations

Nov. 12, 2024
By Lee Landenberger
Flare Therapeutics Inc. will receive $70 million in cash up front from Roche Holding AG, and the deal could ultimately bring the company about $1.8 billion plus royalties. Flare will search for small molecules that can be used to treat undruggable transcription factors to treat cancer. Also, Novartis AG will pay computational-chemistry expert Schrödinger Inc. $150 million up front and as much as $2.3 billion in milestones to develop several candidates along with up to $892 million in R&D and milestone payments.
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3D illustration of kidney cross section

Otsuka says IgAN, too, with phase III sibeprenlimab data

Oct. 29, 2024
By Marian (YoonJee) Chu
Visterra Inc., a subsidiary of Otsuka Pharmaceutical Co. Ltd., reported positive top-line data from the ongoing Visionary phase III study of sibeprenlimab, an anti-APRIL monoclonal antibody for immunoglobulin A nephropathy (IgAN).
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South Korean won

Cellbion the latest radiopharma contender with Kosdaq IPO

Oct. 29, 2024
By Marian (YoonJee) Chu
Cellbion Co. Ltd. debuted on the tech-heavy Kosdaq board of the Korea Exchange Oct. 16, with share prices closing upward at ₩20,650 (US$14.94) – outdoing its initial price of ₩15,000 per share for 1.9 million shares.
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Art concept for molecular glue degradation

Monte Rosa, Novartis have one in VAV1, sign $2.1B pact

Oct. 28, 2024
By Randy Osborne
An old target that found new life at Monte Rosa Therapeutics Inc. has become the subject of a sizeable deal between the company and Novartis AG, as the pair set about developing molecular glue degraders (MGDs). Shares of Monte Rosa (NASDAQ:GLUE) closed Oct. 28 at $9.48, up $4.59, or 93.9%, on word of the Boston-based firm’s deal with Novartis to advance VAV1 MGDs, including MRT-6160, a prospect undergoing a phase I single ascending dose/multiple ascending dose study in healthy volunteers for immune-mediated conditions.
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3D illustration of kidney cross section

Otsuka says IgAN, too, with phase III sibeprenlimab data

Oct. 25, 2024
By Marian (YoonJee) Chu
Visterra Inc., a subsidiary of Otsuka Pharmaceutical Co. Ltd., reported positive top-line data from the ongoing Visionary phase III study of sibeprenlimab, an anti-APRIL monoclonal antibody for immunoglobulin A nephropathy (IgAN).
Read More
Concept art for adeno-associated viral-based gene therapy.

Dyno has another AAV deal, its second with Roche for $1B

Oct. 25, 2024
By Lee Landenberger
Privately held Dyno Therapeutics Inc. has added another notch to its adeno-associated virus (AAV) vectors development portfolio in a deal with the Roche Group that includes $50 million up front and ultimately could top $1 billion. Dyno will help in developing next-generation AAV vectors, optimized by artificial intelligence, to target neurological diseases.
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Concept art for adeno-associated viral-based gene therapy.

Dyno has another AAV deal, its second with Roche for $1B

Oct. 24, 2024
By Lee Landenberger
Privately held Dyno Therapeutics Inc. has added another notch to its adeno-associated virus (AAV) vectors development portfolio in a deal with the Roche Group that includes $50 million up front and ultimately could top $1 billion. Dyno will help in developing next-generation AAV vectors, optimized by artificial intelligence, to target neurological diseases.
Read More
South Korean won

Cellbion the latest radiopharma contender with Kosdaq IPO

Oct. 23, 2024
By Marian (YoonJee) Chu
Cellbion Co. Ltd. debuted on the tech-heavy Kosdaq board of the Korea Exchange Oct. 16, with share prices closing upward at ₩20,650 (US$14.94) – outdoing its initial price of ₩15,000 per share for 1.9 million shares.
Read More

FDA issues CRL: Inspection woes hold up Camurus’ acromegaly drug

Oct. 22, 2024
By Karen Carey
Camurus AB received a complete response letter (CRL) from the U.S. FDA for CAM-2029 (octreotide), its extended-release injection for acromegaly, due to “facility-related deficiencies” identified during a cGMP inspection of a third-party manufacturer. The Lund, Sweden-based company noted that the CRL did not indicate any concerns related to clinical efficacy or safety. Camurus will work with the FDA and the third-party manufacturer to address the concerns, said Fredrik Tiberg, president and CEO.
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Breast cancer illustration

FDA gives early nod to Genentech’s first-line breast cancer drug

Oct. 11, 2024
By Lee Landenberger
Genentech Inc. didn’t need to wait until Thanksgiving for the U.S. FDA to make up its mind. More than a month ahead of its PDUFA date, the agency approved the firm’s first-line breast cancer treatment, Itovebi (inavolisib), providing the oral therapy a place with other niched therapies from Astrazeneca plc and Novartis AG. Itovebi is to be combined with Pfizer Inc.’s palbociclib (Ibrance) and Faslodex (fulvestrant, Astrazeneca) for adults with endocrine-resistant, PIK3CA-mutated, hormone receptor (HR)-positive, HER2-negative, locally advanced or metastatic breast cancer.
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