Author

@OzmosiHealth OzmosiHealth

grade Ccorporatex.com/OzmosiHealth ↗

Real-time biotech catalyst and regulatory event feed across hundreds of clinical-stage names

Publishes a structured, link-backed stream of biotech/pharma

trader score
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hit rate
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mean α
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signals 14d
99

Grade = how their written analysis reads (A best). Trader score = how their last-20 timestamped calls performed vs SPY.

Their picks, scored

Not yet in the scored-bets universe (fewer than 20 scoreable calls). Their last-14d mentions, direction-adjusted, have moved +1.1% since posting (mean over 24 mentions with price data).

Recent signals15receipts included
date (PT)tickerauthorsentwhat they saidsince thenreceipt
2026-08-28CAPR@OzmosiHealth-0.50Reports an FDA review extension amid a securities class action and lead-plaintiff deadline.·
2026-08-28CRSP@OzmosiHealth+0.55Phase 1a data show deep, durable editing and triglyceride and LDL reductions.
2026-08-284568@OzmosiHealth+0.25Daiichi Sankyo presents new real-world bempedoic-acid effectiveness data.·
2026-08-28RHHBY@OzmosiHealth+0.45Roche reports sustained two-year Vabysmo results in difficult-to-treat nAMD.
2026-08-28QNRX@OzmosiHealth+0.55Quoin reports positive interim Phase 2/3 data for QRX003.·
2026-08-28LLY@OzmosiHealth+0.50FDA approves Mounjaro to reduce cardiovascular risk in adults with type 2 diabetes.
2026-08-28OSE@OzmosiHealth+0.00Announces a September 2, 2026 KOL webcast concerning lusvertikimab.·
2026-08-27ACET@OzmosiHealth+0.50FDA cleared Adicet Bio's IND application for ADI-212.·
2026-08-27OTLK@OzmosiHealth+0.10Outlook Therapeutics appointed Kevin Lundquist as CFO.+0.6%
2026-08-27ROIV@OzmosiHealth+0.50FDA approved LISRAYA for adults with dermatomyositis.·
2026-08-27ROIV@OzmosiHealth+0.50FDA approved LISRAYA for adults with dermatomyositis.·
2026-08-27ROIV@OzmosiHealth+0.50Priovant announced FDA approval of LISRAYA for adult dermatomyositis.·
2026-08-27ROIV@OzmosiHealth+0.50Priovant announced FDA approval of LISRAYA for adult dermatomyositis.·
2026-08-27DTIL@OzmosiHealth+0.05Reports presentation of updated OTC-HOPE clinical data at SSIEM 2026.·
2026-08-27ABBV@OzmosiHealth+0.15AbbVie submitted an EMA regulatory application for SKYRIZI induction therapy.-1.0%

Grade is our human read-worthiness rating; trader score is a rolling 20-bet hit-rate/alpha composite — different things, often disagreeing. “Since then” is direction-unaware in the table; the summary line above adjusts for which way they leaned.