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8-K ·Filed Oct 14, 2026

ELVN

Enliven Therapeutics, Inc.
NEUTRAL
Impact 3/10
Horizonweeks Processed11d 18h ago SEC0001193125-26-421761
8-K context-dependent: Items 5.02, 7.01
Actionable Insight • Neutral

The Phase 3 trial initiation timeline (before year-end 2026) is the key catalyst to monitor. No financial data or guidance was provided in this filing.

DirectionNeutral
Confidencehigh
Horizonweeks
Latest settled — T+5d
ELVN ▲ +6.61% at T+5d
NEUTRAL call +6.61% · α vs SPY +7.63% · entry $39.33 → $41.93
Next anchor: T+20d in 16d
Latest observation: T+6 +5.10% FF3 residual α
Entry = T+0 close
Oct 14, 2026
via day close
T+1d
-5.11%
call -5.11% · α -4.00%
$37.32
settled 11d ago
T+5d
+6.61%
call +6.61% · α +7.63%
$41.93
settled 5d ago
T+20d
Pending
in 16d
T+60d
Pending
in 3mo

Price Chart

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Executive Summary

Enliven Therapeutics appointed Kristine Ball to its Board of Directors, effective October 14, 2026, and disclosed plans to initiate the pivotal Phase 3 trial of relcobatinib (ELVN-001) before year-end 2026. The appointment adds commercial-stage biopharmaceutical experience as the company transitions toward late-stage development and potential commercialization. No financial results or material changes to operations were reported.

Key Facts

  • Board expanded from seven to eight directors; Kristine Ball appointed as Class II director and Audit Committee member.
  • Ball receives $45,000/year as outside director plus $10,000/year for Audit Committee service.
  • Ball granted stock options with grant date fair value of approximately $650,000, vesting monthly over 36 months.
  • Company plans to initiate pivotal Phase 3 trial of relcobatinib (ELVN-001) in previously treated CML before year-end 2026.
  • FDA alignment on final design of ENABLE-2 trial was previously announced.

Financial Impact

Director compensation: $55,000 annual cash + ~$650,000 in stock option grant. No impact on revenue or earnings.

Risk Factors

  • Clinical trial risks: relcobatinib may fail to demonstrate sufficient safety, efficacy, or differentiated benefit.
  • Regulatory risks: FDA may disagree with trial design, endpoints, or require additional studies.
  • Financing risk: company may need additional capital to fund operations and clinical development.

Investment Themes

Biotech & Drug Discovery

Documents Analyzed

This report is based on 5 SEC documents filed with EDGAR.

DocumentAccession Number
8-K Filing (Primary)0001193125-26-421761
Document: d13112dex991.htm0001193125-26-421761
Document: 0001193125-26-421761-index-headers.html0001193125-26-421761
Document: 0001193125-26-421761-index.html0001193125-26-421761
Document: 0001193125-26-421761.txt0001193125-26-421761
18 reports for ELVN
Performance horizon
40% Hit rate @ T+5 2 of 5 directional calls Went positive at some point 3 of 5 best @ T+60▲ +46.98%Jun 11, 2026
Filters
Rows
Reports for ELVN — sortable, filterable
TypeNow
Oct 21, 2026
4d ago
Insider Cluster
NEUTRAL ★ 3/10
$41.93awaiting T+5—$41.29 (−1.53%)
Oct 19, 2026
6d ago
144
NEUTRAL ★ 2/10
$41.25awaiting T+5—$41.29 (+0.10%)
Oct 16, 2026
9d ago
3
NEUTRAL ★ 2/10
$38.70awaiting T+5—$41.29 (+6.69%)
Oct 14, 2026
11d ago
8-K
NEUTRAL ★ 3/10
$39.33 $41.93▲ +6.61%▲ +7.63%$41.29 (+4.98%)
Sep 21, 2026
4w ago
Insider Cluster
NEUTRAL ★ 2/10
$48.19 $46.51▼ −3.49%▼ −2.30%$41.29 (−14.32%)
Sep 4, 2026
7w ago
144
NEUTRAL ★ 3/10
$59.32 $54.43▼ −8.24%▼ −7.03%$41.29 (−30.39%)
Aug 19, 2026
9w ago
Insider Cluster
NEUTRAL ★ 2/10
$58.97 $60.50▲ +2.59%▲ +1.48%$41.29 (−29.98%)
Aug 9, 2026
11w ago
Institutional Cluster
BULLISH ★ 6/10
$59.42 $59.54▲ +0.19%▲ +0.24%$41.29 (−30.51%)
Jul 21, 2026
13w ago
Insider Cluster
NEUTRAL ★ 2/10
$52.85 $52.97▲ +0.23%▲ +2.63%$41.29 (−21.87%)
Jun 22, 2026
17w ago
144
NEUTRAL ★ 2/10
$48.60 $50.85▲ +4.63%▲ +3.62%$41.29 (−15.04%)
Showing 10 of 18

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Report published Oct 14, 2026