This page shows the latest Lartruvo news and features for those working in and with pharma, biotech and healthcare.
Authorisation revoked for Lartruvo. Friday’s ruling was also notable for the CHMP’s decision to revoke the marketing authorisation for Eli Lilly’s sarcoma treatment Lartruvo, after the drug failed
Existing patients can use access programme. Eli Lilly is to withdraw its soft tissue sarcoma treatment Lartruvo from the market after it failed a post-marketing efficacy study. ... The trial studied Lartruvo combined with standard treatment doxorubicin,
Lilly said at the time it would stop promoting Lartruvo and would book a $70m-$90m charge this quarter as a result. ... Meanwhile, the trial failure also impacts Lartruvo in the US, as the FDA also approved the drug early on the promise of follow-up data.
Licensed for use with doxorubicin for soft tissue sarcoma patients. The European Commission has granted Lilly's Lartruvo (orlaratumab) marketing authorisation for the first-line treatment of patients with advanced soft ... Until then, Lartruvo will be
Eli Lilly has picked up its first green light for its soft tissue sarcoma (STS) therapy Lartruvo, ending a four-decade drought for new front-line therapies. ... The US FDA granted accelerated approval to Lartruvo (olaratumab) used in combination with
Eli Lilly could be just weeks away from EU approval of its advanced soft tissue sarcoma (STS) treatment Lartruvo after a positive recommendation from the Committee for Medicinal Products for Human ... It is thought that by binding to the receptor
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Among the noteworthy approvals are Lartruvo (for the treatment of soft tissue sarcoma, approved in the EU and US), Rubraca (for the treatment of ovarian cancer, only approved in the US),
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