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FDA expands Altor's Ankitva use to papillary bladder cancer
The U.S. Food and Drug Administration (FDA) has received a supplemental biologics license application (sBLA) for nogapendekin alfa inbakicept-pmln (Anktiva), expanding its potential use to treat patients with Bacillus Calmette–Guérin (BCG)–unresponsive non–muscle-invasive bladder cancer (NMIBC)…
AInvest Wire · 22h agoMonkeypox stocks rose in intraday trading, with EBS up 17.9%, GOVX gaining 24.3% and MRNA rising 6.7%.
On October 5, 2026, stocks linked to monkeypox vaccine development saw significant intraday gains amid ongoing global health concerns. EBS surged 17.9%, while GOVX climbed 24.3%, and MRNA rose 6.7%. These movements reflect heightened investor interest in biotechnology firms positioned to benefit…
AInvest Wire · Oct 5, 2026Regeneron Pharmaceuticals: Serious TEAEs grade 3+ in 21% of LGSOC patients; TEAEs in 74%; neutropenia, anemia, elevated liver enzymes
Regeneron Pharmaceuticals' MEK inhibitor binimetinib, evaluated in the phase III MILO trial for recurrent or persistent low-grade serous ovarian cancer (LGSOC), demonstrated notable toxicity profiles. The trial reported that 74% of patients experienced treatment-emergent adverse events (TEAEs),…
AInvest Wire · Oct 1, 2026Regeneron Pharmaceuticals: TEAEs occurred in 100% of LGSOC patients; cytokine release syndrome in 90%, all grade 1 or 2
Regeneron Pharmaceuticals recently reported preliminary data from a clinical trial involving patients with low-grade serous ovarian cancer (LGSOC). The study indicated that treatment-emergent adverse events (TEAEs) occurred in 100% of participants, with cytokine release syndrome observed in 90% of…
AInvest Wire · Oct 1, 2026Eli Lilly - Treatment-emergent adverse events in 41.8% eBGLySS patients, 39.6% placebo, all mild or moderate
AInvest Wire · Sep 30, 2026Light Horse does not author, endorse or verify the headlines, and their appearance here is not an endorsement of any view they express.
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