IMVT-1402 at 600 mg hit its primary endpoint in difficult-to-treat rheumatoid arthritis, with 92.5% of patients maintaining ACR20 response, and FDA talks on a registrational path come later this year. The 300 mg dose failed to separate from placebo and secondary endpoints missed significance, so the agency meeting decides how much of that $6.3 billion valuation holds.
Latest Activity
IMVT Coverage
Share Offerings Prompt Huge Insider Buying in These 3 Biotechs
Secondary offerings from biotechs Immunovant, Kymera Therapeutics, and Wave Life Sciences prompted some huge insider buying recently.