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RECURSION PHARMACEUTICALS, INC. logo

RXRX

NASDAQSALT LAKE CITY, UT
RECURSION PHARMACEUTICALS, INC.

Recursion is a clinical-stage TechBio company developing small molecule drugs across multiple therapeutic areas using its Recursion Operating System, an AI-native platform that integrates biological data generation, AI-powered molecular synthesis, and AI-enabled clinical development. The company has demonstrated clinical validation with a positive readout in its familial adenomatous polyposis program using a MEK1/2 inhibitor, along with multiple clinical-stage and preclinical programs differentiated by novel biology and chemistry insights. Recursion has established strategic partnerships with companies including Roche, Genentech, and Sanofi, and has received over $500 million in partner payments for novel data generation and AI-designed small molecule program advancement.

$3.46-38.10%1Y
RXRX · daily close · illustrative · 0 catalysts marked
1Y high$6.791Y low$2.84range$3.95(139%)past catalysts

Pipeline3

Phase 2Head and Neck Squamous Cell Carcinoma (HNSCC)
Phase 2Pancreatic Adenocarcinoma
Phase 2Platinum-resistant High-grade Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancers (HGSOC)
Phase 2Hormone Receptor Positive [HR+] and Human Epidermal Growth Factor Receptor 2 Negative [HER2-] Breast Carcinoma
Phase 2Triple Negative Breast Cancer (TNBC)
Phase 2Non-Small Cell Lung Cancer
small-molecule
Phase 2Head and Neck Squamous Cell Carcinoma (HNSCC)
Phase 2Pancreatic Adenocarcinoma
Phase 2Platinum-resistant High-grade Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancers (HGSOC)
Phase 2Hormone Receptor Positive [HR+] and Human Epidermal Growth Factor Receptor 2 Negative [HER2-] Breast Carcinoma
Phase 2Triple Negative Breast Cancer (TNBC)
Phase 2Non-Small Cell Lung Cancer
small-molecule
UnknownIndication pending review

Catalyst Calendar1

Past (1)
SEP 03
2024
ReadoutREC-994
On September 3, 2024, the Company issued a press release announcing top-line results of its SYCAMORE trial, a 12-month Phase 2 randomized double-blind, placebo-controlled, safety, tolerability and exploratory efficacy study for REC-994 in symptomatic cerebral cavernous malformation patients.
8-K

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