This page shows the latest Trevena news and features for those working in and with pharma, biotech and healthcare.
FDA sets review completion date of 7 August 2020. US biotech Trevena has resubmitted its lead drug oliceridine for moderate-to-severe pain in the US, 18 months after it was ... The new review – which the FDA considers a class two resubmission so will
BMIs. Meanwhile, Trevena’s intravenous opioid olicerdine for the management of moderate-to-severe acute pain in adult patients narrowly missed out on a recommendation from the committee, with eight members
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in the EU and US last year but still in development); Allergan/Trevena's AT1 receptor antagonist TRV207l and off-patent compound perhexiline, thought to improve the efficiency of heart muscle
Biotechs including Xencor, Trevena and Vital Therapies have also postponed their IPOs citing unfavourable market conditions.
75. Trevena. TRV027, GPCR biased ligand for acute heart failure (phase II).
Rare disease medicines $76m sales. 693. Trevena/ Forest . Option to license equity.
The deals that fall into this category are: Forest's $460m option to license a phase II acute heart failure treatment from Trevena; Merck's $430m licence of diabetes type 2
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Trevena Pharmaceuticals.
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