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BioWorld - Thursday, February 5, 2026
Home » Newsletters » BioWorld

BioWorld

Jan. 10, 2022

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Gold dollar sign inside gold cog

Century’s $3.25B deal with BMS is the biggest of four new $1B+ collaborations

Century Therapeutics Inc.’s $3.25 billion deal with Bristol Myers Squibb Co. (BMS) was the largest of four billion-dollar-plus agreements announced Dec. 10, piggybacking on a busy week that includes the start of the 40th annual J.P. Morgan Healthcare Conference. Read More

2022 deals kick into gear with tide of $1B+ gene and RNA therapy collaborations

A raft of potentially high-value drug development collaborations, most for gene and RNA therapies, led the first day of the 40th Annual J.P. Morgan Healthcare Conference Monday. Pfizer Inc. enlisted Beam Therapeutic Inc. to advance in vivo base editing programs for up to $1.35 billion, while Bayer AG tapped Mammoth Biosciences Inc.’s in vivo CRISPR systems expertise in a potential $1 billion-plus deal. Selecta Biosciences Inc. inked a new $1.1 billion partnership with Ginkgo Bioworks Inc. to develop next-generation gene therapy capsids, while Acadia Pharmaceuticals Inc. agreed to pay Stoke Therapeutics Inc. as much as $967 million to develop RNA-based medicines. Work on new mRNA vaccines and therapies is also proceeding, with both Pfizer and Biontech SE announcing new collaborations in the space. Read More
Insomnia

Idorsia gains first ever FDA approval for insomnia drug Quviviq

After 25 years of research. Allschwil, Switzerland’s Idorsia Ltd. has had its first drug approved by the FDA – Quviviq (daridorexant) for adults with insomnia. The okay for Quviviq is the result of painstaking research led by the firm’s chief scientific officer, Martine Clozel, whose husband Jean-Paul Clozel is CEO. Read More

Durable goods? Biomarin ‘rox’ in hemophilia A with two-year gene therapy data

Having unveiled more data from the ongoing, global phase III Gener8-1 study with Roctavian (valoctocogene roxaparvovec, also known as valrox), Biomarin Pharmaceutical Inc. remains on track to file a regulatory submission with the FDA in the second quarter of this year for the gene therapy to treat adults with severe hemophilia A. The EMA is already reviewing a marketing authorization application. Read More
Aduhelm product image

US CMS decision could mark future for Alzheimer’s drugs

This could be a make-or-break week for Biogen Inc., with the U.S. Centers for Medicare & Medicaid Services (CMS) expected to announce a draft coverage decision for the company’s Alzheimer’s drug, Aduhelm. Read More
Drugs to Watch 2022 report cover

Drugs to Watch 2022: Seven drugs expected to be blockbusters

The pandemic has forced pharma and biotech to be more agile to better navigate the obstacles and still find success. Supply chain gaps are part of the problem, as are clinical trial delays. Yet the industry has successfully forged ahead in the past year to produce the seven drugs Clarivate believes in the next five years will each earn more than $1 billion annually. Read More
T cells

Study shows cross-protection of common cold T cells against SARS-CoV-2

LONDON – T cells generated as a result of infection with common cold coronaviruses provide cross-protection against being infected with SARS-CoV-2, according to a new study. Read More

Rare slate of FDA leaders ponders challenges, agency's future

FDA commissioners past, present and likely future gathered together for a rare joint discussion Jan. 9, as part of the third annual Innovations in Regulatory Science Summit. Read More

Prism offers Genentech peptide mimetic small-molecules library for multitarget collaboration

Prism Biolab Co. Ltd. has added Genentech Inc., a unit of Roche Holding AG, to the list of users for its peptide mimetic small-molecules library after signing a multitarget research collaboration and licensing agreement. Under the agreement, Tokyo-based Prism Biolab will open its Pepmetics Library, a library of peptide mimetic small molecules, to screen against targets selected by Roche and Genentech. Read More

Kyowa Kirin expands Inveniai AI platform collaboration once again

Inveniai LLC and Kyowa Kirin Co. Ltd. have expanded their partnership a second time, inking their most recent multiple drug discovery agreement. The multiyear deal will see the duo discover novel targets and treatments for therapeutic areas across Kyowa Kirin’s portfolio and areas of interest using Inveniai’s artificial intelligence (AI) platform. Read More
ICYMI illustration

ICYMI: Week in review, Jan. 3-7, 2022

A quick look back at top stories. Read More

Appointments and advancements for Jan. 10, 2022

New hires and promotions in the biopharma industry, including: Asklepios, Autolus, Avicanna, Eyepoint, Foghorn, H3, Iovance, JW, Karyopharm, Madrigal, Omega, Poseida, Recode, Sesen. Read More

Financings for Jan. 10, 2022

Biopharmas raising money in public or private financings, including: Cellusion, Delix, Intra-Cellular, KKR, Maze. Read More

In the clinic for Jan. 10, 2022

Clinical updates, including trial initiations, enrollment status and data readouts and publications: 4D, Biocryst, Biosight, Deinove, Golden, Noxxon, Nuvalent, Oxurion, Recce, Revive. Read More

Other news to note for Jan. 10, 2022

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Abbvie, Acelrx, Acerus, Acuitas, Adaptate, Aptorum, Biohaven, Biomea, Carisma, Castle Creek, Catalyst, Coherus, Cullinan, Cytodyn, Dinaqor, Esocap, Everest, Frontier, Gilead, High Line Bio, Iksuda, Jacobus, Junshi, Kriya, Legochem, Lowell, Merck KGaA, Moderna, Mydecine, Neoleukin, Novavita, Pfizer, Philogen, Regnum, Remedium, Sevenscore, Takeda, Trialspark, Upadia, Verity, Warden. Read More

Regulatory actions for Jan. 10, 2022

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Dynacure, Moderna, Paxmedica.

Read More

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