ORIC
ORIC Pharmaceuticals, Inc.9.12
-0.11-1.19%
Dec 16, 4:00:01 PM EST
Earnings Call Transcripts
This Quarter (Q1 '26)
No earnings call transcript available yet
Last Quarter (Q4 '25)
No earnings call transcript available
Key Stats
Market Cap
888.19MP/E (TTM)
-Basic EPS (TTM)
-1.71Dividend Yield
0%Recent Filings
8-K
Rinzimetostat Phase 3 dose selected
ORIC unveiled Phase 1b dose optimization data for rinzimetostat (ORIC-944) plus darolutamide in post-abiraterone mCRPC on March 31, 2026, selecting 400 mg QD as the provisional Phase 3 dose. It showed 93% 3-month rPFS, 84% at 4- and 5-months, 47% PSA50 responses, and 71% ctDNA reductions—competitive efficacy yet far cleaner safety with mostly Grade 1/2 AEs and no dose reductions at 400 mg. Himalayas-1 Phase 3 launches 1H 2026. Data immature.
8-K
New $200M ATM prospectus filed
ORIC Pharmaceuticals filed a new prospectus supplement on February 26, 2026, enabling up to $200 million in additional at-the-market share sales via Jefferies under its 2025 Sales Agreement. It exhausted the prior 2024 supplement after selling 13,478,432 shares for $139.7 million gross proceeds as of February 23. Fresh capital pipeline unlocked. Legal opinion supports the offering.
8-K
ORIC posts strong trial data
ORIC Pharmaceuticals reported Q4 and full-year 2025 results, highlighting Phase 1b data for rinzimetostat showing 55% PSA50 responses in mCRPC and enozertinib's 67-80% ORR plus 100% intracranial ORR in NSCLC. Cash hit $392.3M, bolstered by $264M raised, funding ops into 2H 2028. Multiple readouts loom in 2026. Cash extends runway.
10-K
FY2025 results
Oric Pharmaceuticals advanced its clinical pipeline through FY2025 ended December 31, 2025, prioritizing rinzimetostat and enozertinib after August 2025 preclinical cuts. Q4 momentum surged with November Phase 1b data for rinzimetostat in mCRPC, showing 55% PSA50 responses and 59% ctDNA clearance across doses with apalutamide or darolutamide; safety stayed clean, no Grade 4/5 AEs. December brought enozertinib Phase 1b updates at ESMO Asia, confirming 80mg QD for Phase 3 with strong CNS activity in EGFR exon 20/ PACC NSCLC. Pipeline sharpened. Clinical delays threaten timelines.
8-K
Enozertinib Phase 1b data beats benchmarks
ORIC unveiled Phase 1b data for enozertinib on December 6, 2025, showing 45% confirmed ORR in 2L EGFR exon 20 NSCLC and 36% in pretreated EGFR PACC, beating benchmarks, with 100% intracranial ORR in 1L settings including active brain metastases. Safety proved solid at 80 mg QD, the picked dose for potential Phase 3. Data mature mid-2026. Risks loom in trials.
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