0.00Open0.00Pre Close0 Volume0 Open Interest10.00Strike Price0.00Turnover0.00%IV135.29%PremiumNov 15, 2024Expiry Date0.00Intrinsic Value100Multiplier11DDays to Expiry0.00Extrinsic Value100Contract SizeAmericanOptions Type--Delta--Gamma5.67Leverage Ratio--Theta--Rho--Eff Leverage--Vega
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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