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BioWorld - Tuesday, January 13, 2026
Home » Topics » Immune, BioWorld

Immune, BioWorld
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3D illustration of human digestive system

OSE’s IL-7 therapy hits mark in ulcerative colitis trial

Nov. 5, 2024
By Nuala Moran
OSE Therapeutics SA has reported positive data for lusvertikimab in a phase II trial in ulcerative colitis, boosting the monoclonal antibody’s prospects of becoming the first anti-interleukin-7 therapy to reach the market.
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Female doctor and patient

BioFuture 2024: Half the population’s health needs are underserved

Nov. 4, 2024
By Lee Landenberger
While the size of the market is enormous, drug development and treatments for women’s health care still lag behind what is offered for men. There has been a renaissance in the past few years, however, led by investors and companies that have wrestled with determining exactly what encompasses women’s health and how to meet its challenges.
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AI-generated digital horse illustration
Cancer

Gene editing is Trojan horse of cancer immunotherapy

Nov. 4, 2024
By Mar de Miguel
Gene editing strategies, from epigenetic engineering to cell reprogramming and genetic vaccines, are accelerating the development of new therapies that awaken the immune system to treat cancer, as presented last month in Rome at the 31st Annual Congress of the European Society of Gene and Cell Therapy (ESGCT). Some of these advances are taking advantage of the conditions of the tumor microenvironment, where cancer cells coexist with immune cells, microorganisms and blood vessels.
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Tharimmune surges on phase II plans in liver disease pruritus

Oct. 30, 2024
By Jennifer Boggs
Shares of Tharimmune Inc. shot up more than 100% in early trading Oct. 30 as the firm disclosed regulatory backing to launch a phase II trial this quarter testing TH-104, a transdermal buccal film version of nalmefene, to treat pruritus that is associated with primary biliary cholangitis.
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Blue dollar sign on white background

Synox extends series B by $17B to advance emactuzumab

Oct. 30, 2024
By Nuala Moran
Synox Therapeutics Ltd. extended its series B by a further $17 million as it announced the first patients have been dosed in a phase III study of emactuzumab in the treatment of tenosynovial giant cell tumor, a rare condition in which benign tumors grow in the soft tissue lining of joints and tendons.
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Biogen, Neomorph pact worth $1.45B for molecular glue degraders

Oct. 30, 2024
By Karen Carey
Two days after Monte Rosa Therapeutics Inc. signed a molecular glue degrader deal with Novartis AG, two other companies, Biogen Inc. and Neomorph Inc., are moving forward in the same space in a partnership worth up to $1.45 billion. Cambridge, Mass.-based Biogen and San Diego-based Neomorph will develop molecular glue degraders (MGDs) for priority targets in Alzheimer’s, rare neurological and immunological diseases, using Neomorph’s MGD platform to identify and validate novel small-molecule protein degraders.
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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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Gold dollar sign and gray question marks

Uncertainties plague short-term ‘win’ of US price negotiations

Oct. 25, 2024
By Mari Serebrov
If the maximum fair prices the U.S. CMS announced after the first round of drug price negotiations are any indication, advocates of the government price setting may be settling for short-term wins at the cost of long-term, more sustainable price reductions driven by competition.
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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).
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DBV making sure peanut-allergy patch plan sticks with FDA

Oct. 23, 2024
By Randy Osborne
DBV Technologies SA CEO Daniel Tasse said his firm will meet “very shortly” with the U.S. FDA for talks that will formalize an accelerated approval process for the Viaskin Peanut allergy patch. “Did this take longer than expected? Yes, it did,” Tasse said during a conference call update. “But this was a choice we made, and it was a necessary choice” in order to nail down precise requirements for the product.
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