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REGN

FDA Approves Regeneron’s ARCALYST™ (rilonacept) for Treatment of Cryopyrin-Associated Periodic Syndromes (CAPS) First therapy approved for this rare, hereditary, inflammatory disease Regeneron to host conference call on Thursday morning, February 28, 2008 at 8:30 a.m. Eastern Time

Friday, February 29, 2008 BiopharmaWatch Research 1 min read
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Key Takeaway: FDA Approves Regeneron’s ARCALYST™ (rilonacept) for Treatment of Cryopyrin-Associated Periodic Syndromes (CAPS) First therapy approved for this rare, hereditary, inflammatory disease Regeneron to host conference call on Thursday morning, February 28, 2008 at 8:30 a.m. Eastern Time

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+35%
120-day peak, hindsight
Typical move
2.6%
average across 15 past catalysts
Lead asset
VEGF Trap-Eye
Phase 1 · Diabetic Macular Edema

Full Press Release Details

FDA Approves Regeneron’s ARCALYST™ (rilonacept) for Treatment of Cryopyrin-Associated Periodic Syndromes (CAPS) First therapy approved for this rare, hereditary, inflammatory disease Regeneron to host conference call on Thursday morning, February 28, 2008 at 8:30 a.m. Eastern Time.
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Last updated: Feb 29, 2008

Biotech snapshot

Cash runway
$17823M liquidity · $0M/mo burn
Low dilution risk
Lead asset
VEGF Trap-EyePhase 1
Diabetic Macular Edema →

Catalyst track record

+35%
best trade around REGN's most recent catalyst

Peak hindsight return over a 120-day window, across 15 tracked FDA/PDUFA catalysts for REGN.

See every catalyst's timing & PoA →