MARKET

ELVN

ELVN

Enliven Therapeutics Inc
NASDAQ
21.40
+0.40
+1.90%
After Hours: 21.40 0 0.00% 16:10 12/04 EST
OPEN
20.97
PREV CLOSE
21.00
HIGH
21.79
LOW
20.57
VOLUME
494.58K
TURNOVER
--
52 WEEK HIGH
25.96
52 WEEK LOW
13.30
MARKET CAP
1.27B
P/E (TTM)
-11.5945
1D
5D
1M
3M
1Y
5Y
1D
Enliven Therapeutics (ELVN): Assessing Valuation After a Recent 13% Share Price Rebound
Simply Wall St · 50m ago
Wall Street Analysts Believe Enliven Therapeutics, Inc. (ELVN) Could Rally 101.26%: Here's is How to Trade
NASDAQ · 1d ago
Weekly Report: what happened at ELVN last week (1124-1128)?
Weekly Report · 3d ago
Weekly Report: what happened at ELVN last week (1117-1121)?
Weekly Report · 11/24 10:38
Enliven Therapeutics Chief Scientific Officer Joseph P. Lyssikatos Reports Sale of Common Shares
Reuters · 11/21 22:28
Enliven Therapeutics CEO Samuel Kintz Reports Disposal of Common Shares
Reuters · 11/19 23:45
Enliven Therapeutics (ELVN): Assessing Valuation Following ENABLE Trial Milestone and Renewed Analyst Optimism
Simply Wall St · 11/18 20:42
Enliven Therapeutics: Notable Early Signals, But Too Many Assumptions To Justify A Buy
Seeking Alpha · 11/18 12:55
More
About ELVN
Enliven Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on the discovery and development of small molecule inhibitors to help patients with cancer. It is advancing two parallel lead product candidates, ELVN-001 and ELVN-002, and pursuing several additional research stage opportunities that align with its development approach. Its first product candidate, ELVN-001, is a potent, highly selective, small molecule kinase inhibitor designed to specifically target the breakpoint cluster region-Abelson (BCR-ABL) gene fusion, the oncogenic driver for patients with chronic myeloid leukemia. Its second product candidate, ELVN-002, is a potent, highly selective, central nervous system penetrant and irreversible human epidermal growth factor receptor 2 (HER2) inhibitor with activity against wild type HER2 and various HER2 mutations. ELVN-002 is designed to inhibit wild type HER2 and key mutations of HER2, while sparing wild-type EGFR and avoiding EGFR-related toxicities.

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