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BioWorld - Thursday, December 18, 2025
Home » Newsletters » BioWorld

BioWorld

Dec. 8, 2022

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Site hound: Relmada phase III in depression dogged again by placebo hitch

Investigators at Relmada Therapeutics Inc. believe the same problem that plagued an earlier phase III effort called Reliance-3 – an “implausibly” high placebo response at certain sites – also foiled the latest phase III study (conducted at overlapping sites) known as Reliance-1, testing REL-1017 (esmethadone), meant as an adjunctive treatment for major depressive disorder. Read More

Eiger’s D-LIVR study delivers the composite endpoint but stock stumbles

Top-line primary data from week 48 of Eiger Biopharmaceuticals Inc.'s phase III D-LIVR study of lonafarnib, a prenylation inhibitor for treating chronic hepatitis delta virus, also known as hepatitis D, hit statistical significance vs. a placebo in the composite primary endpoint. Read More
Vevo Therapeutics team

Vevo raises $12M seed round for in vivo screening of pooled cancer cells

Vevo Therapeutics Inc. raised $12 million in an over-subscribed seed round to build out an in vivo single-cell screening platform, which will enable it to interrogate simultaneously the effects of small molecule drug leads on multiple cancer cell lines. Read More

China grants emergency use of new vaccines as it eases COVID-19 policy

China recently approved four COVID-19 vaccines for emergency use in a span of two days. The nods were granted to Clover Biopharmaceuticals Ltd., Sinocelltech Group Ltd., Beijing Wantai Biological Pharmacy Enterprise Co. Ltd. and Westvac Biopharma Co. Ltd. There is still no mRNA vaccine approved in the country. Read More
3d illustration of ovarian cancer

Compugen reports phase I data for anti-PVRIG candidate

At the ESMO Immuno-Oncology Congress 2022, Compugen Inc. shared phase I data for COM-701 in dual and triple combination with Bristol Meyers Squibb Co.’s Opdivo (nivolumab) and with or without BMS-986207. Compugen’s candidate demonstrated preliminary durable antitumor activity and immune activation in patients with platinum resistant ovarian cancer with a favorable safety and toxicity profile. Read More
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The BioWorld Insider Podcast: Looking ahead to 2023, CEOs contemplate the new normal

We wrapped up 2022 and are preparing for 2023 on this BioWorld Insider podcast. Staff writer Lee Landenberger talked to four CEOs, visionaries of companies producing new science and drug development. The CEOs offered their insights into what happened this year and looked at the challenges and opportunities for next year. Read More

Appointments and advancements for Dec. 8, 2022

New hires and promotions in the biopharma industry, including: Anjarium, Domain, Eyenovia, Geovax, Regen, Relief, Tenaya, Wren. Read More

Conference data for Dec. 8, 2022: ESMO

New and updated clinical data presented by biopharma firms at the ESMO Immuno-Oncology Congress 2022, including: Immunocore, Jounce, NGM, Promontory, Rapt. Read More

Financings for Dec. 8, 2022

Biopharmas raising money in public or private financings, including: Cabaletta, Celcuity, Dantari, Omeicos, Prometheus, Replimune. Read More

In the clinic for Dec. 8, 2022

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Amo, Avrobio, Axsome, Bio-Path, Boehringer, Ingelheim, Cytokinetics, Daiichi Sankyo, Eli Lilly, Eupraxia, Gilead, KSQ, Medicinova, Neurocrine, Novartis, Ocugen, Pharming, Prometheus, Rani, Replimune, UCB, Vor. Read More

Other news to note for Dec. 8, 2022

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Abiogen, Actinium, Altamedics, Addex, Daiichi Sankyo, Entrada, Gilead, Indivior, Instil, Kite, Revolution, Sanofi, Sensei, Sosei, Spikimm, Tevogen and Vertex. Read More

Regulatory actions for Dec. 8, 2022

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amarin, Ascletis, Delta-Fly, Moleculin, Novavax, Oncopeptides, Qualigen, Sionna. Read More

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