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PRESS-RELEASE ·Filed Apr 21, 2026

BDTX

Black Diamond Therapeutics, Inc
BULLISH
Impact 7/10
Horizonweeks Processed6mo ago WireGlobeNewswire
Press release · FDA
Actionable Insight ▲ Bullish

ASCO presentations in late May–June 2026 could catalyze investor interest, especially if updated efficacy or durability data are presented. Monitor for signs of progression-free survival (PFS) or duration of response (DOR) data, which are key value drivers beyond ORR.

DirectionBullish
Confidencehigh
Horizonweeks
Final — all horizons settled through T+60d
BDTX ▼ -42.54% at T+60d
LONG call ✗ call lost -42.54% · α vs SPY -49.44% · entry $3.15 → $1.81
Entry = T+0 close
Apr 21, 2026
via day close
T+1d
+6.35%
call +6.35% · α +5.33%
$3.35
settled 6mo ago
T+5d
-14.29%
call -14.29% · α -15.37%
$2.70
settled 6mo ago
T+20d
-18.10%
call -18.10% · α -23.01%
$2.58
settled 5mo ago
T+60d
-42.54%
call -42.54% · α -49.44%
$1.81
settled 3mo ago

Price Chart

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Executive Summary

Black Diamond Therapeutics announced upcoming presentations of Phase 2 data for silevertinib in non-small cell lung cancer (NSCLC) and a planned randomized Phase 2 trial in glioblastoma (GBM) at ASCO 2026. The company previously reported strong early results in NSCLC, including a 60% objective response rate and 86% CNS response rate, with no new safety signals.

Key Facts

  • Silevertinib showed 60% ORR and 86% CNS ORR in treatment-naïve NSCLC patients with non-classical EGFR mutations as of November 3, 2025.
  • Phase 2 data will be presented at ASCO 2026 in both oral and poster sessions, increasing scientific visibility.
  • Company is initiating a randomized Phase 2 trial in newly diagnosed EGFRvIII-positive GBM in Q2 2026, indicating clinical advancement.
  • Silevertinib is a brain-penetrant, fourth-generation EGFR inhibitor with activity across >50 non-classical EGFR mutations and EGFRvIII in GBM.
  • Over 200 patients have been treated with silevertinib to date, supporting ongoing development.

Financial Impact

No direct financial impact disclosed, but positive clinical data de-risks development and supports potential future revenue from silevertinib in NSCLC and GBM.

pipeline valueR&D progressmarket sentiment

Risk Factors

  • Forward-looking statements carry high uncertainty; future data may not replicate initial results.
  • Silevertinib remains in mid-stage development with no guarantee of regulatory approval.
  • Company has no approved products and relies entirely on clinical trial outcomes for value creation.

Market Snapshot

Exchange
Nasdaq
Sector
Biological Products, (No Diagnostic Substances)

Investment Themes

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3278175
7 reports for BDTX
Performance horizon

Track record builds as more directional reports settle.

Filters
Rows
Reports for BDTX — sortable, filterable
TypeNow
Aug 15, 2026
10w ago
Institutional Cluster
NEUTRAL ★ 4/10
$2.05 $2.06▲ +0.49%▲ +1.16%$1.69 (−17.56%)
Aug 5, 2026
11w ago
8-K
NEUTRAL ★ 5/10
$1.92 $1.95▲ +1.56%▲ +0.95%$1.69 (−11.98%)
May 21, 2026
22w ago
8-K
BULLISH ★ 7/10
$2.28 $2.33▲ +2.19%▲ +1.61%$1.69 (−25.88%)
May 21, 2026
22w ago
Press Release
BULLISH ★ 8/10
$2.28 $2.33▲ +2.19%▲ +1.61%$1.69 (−25.88%)
May 7, 2026
24w ago
8-K
NEUTRAL ★ 4/10
$2.72 $2.99▲ +9.93%▲ +9.10%$1.69 (−37.87%)
Apr 21, 2026
26w ago
Press Release
BULLISH ★ 7/10
$3.15 $3.35▲ +6.35%▲ +5.33%$1.69 (−46.35%)
Mar 16, 2026
32w ago
Press Release
MIXED ★ 6/10
$2.23 $2.17▼ −2.69%▼ −1.29%$1.69 (−24.22%)
Showing 7 of 7

US Market Status

Market Closed — Opens Tue (16h 36m)

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Report published Apr 21, 2026