0.05Open0.05Pre Close0 Volume21 Open Interest9.00Strike Price0.00Turnover308.95%IV105.22%PremiumNov 15, 2024Expiry Date0.00Intrinsic Value100Multiplier7DDays to Expiry0.05Extrinsic Value100Contract SizeAmericanOptions Type0.0706Delta0.0724Gamma88.20Leverage Ratio-0.0171Theta0.0000Rho6.23Eff Leverage0.0008Vega
Omeros Stock Discussion
FDA Grants Rare Pediatric Disease Designation to Omeros’ MASP-3 Inhibitor Zaltenibart for Treatment of C3 Glomerulopathy
Omeros announced that its MASP-3 inhibitor zaltenibart (OMS906) received rare pediatric disease designation from the FDA for treating C3 glomerulopathy (C3G), an ultra-rare renal disorder affecting children and young adults. The company plans to initiate Phase 3 trials for C3G in 2024. Zaltenibart is also being developed for paroxysmal nocturnal hemoglob...
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7 MINUTES AGO, 9:05 AM EDT
• Proteinuria reduction in the placebo group was substantially greater than reported in other IgA nephropathy clinical trials
• Webcast conference call planned for 8:30 a.m. ET today
Next week big pharma companies such as $Biogen (BIIB.US)$ , $Sage Therapeutics (SAGE.US)$ , and $Ironwood Pharmaceuticals (IRWD.US)$ will release their quarterly earnings report.
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