BDTX Black Diamond Therapeutics, Inc

BULLISH Impact: 8/10 PRESS-RELEASE
Horizon weeks Filed May 21, 2026 Processed 22d 16h ago Wire GlobeNewswire
Press release: fda
Latest settled — T+5d ⚠ clustered
BDTX ▼ -0.88% at T+5d
LONG call ✗ call lost -0.88% · α vs SPY -2.55% · entry $2.28 → $2.26
Next anchor: T+20d in 9d
Currently $1.75 · -23.25% from $2.28 entry
Entry anchored
May 21, 03:59 PM ET
via Databento tick
T+1d
+2.19%
call +2.19% · α +1.61%
$2.33
settled 22d ago
T+5d
-0.88%
call -0.88% · α -2.55%
$2.26
settled 15d ago
T+20d
call — · α —
in 9d
T+60d
call — · α —
in 2mo

Price Chart

Loading chart...

Executive Summary

Black Diamond Therapeutics reported positive Phase 2 results for silevertinib in frontline NSCLC with EGFR non-classical mutations, showing a preliminary median PFS of 15.2 months, 60% ORR, and 86% CNS ORR with no new brain metastases. The company plans to meet with the FDA later this year to discuss a pivotal development plan, positioning silevertinib as a potential practice-changing therapy for an underserved patient population.

Actionable Insight

The strong efficacy and CNS activity data de-risk silevertinib's pivotal path; the upcoming FDA meeting and ASCO presentation on May 30 are key catalysts. Traders should watch for updates on the pivotal trial design and potential partnership interest, as well as the randomized Phase 2 GBM trial initiation.

Key Facts

  • Preliminary median PFS of 15.2 months in 43 patients with 1L NSCLC and EGFR-NCMs
  • ORR of 60% and DCR of 91% by RECIST 1.1
  • 86% CNS ORR in patients with measurable brain metastases; no patients developed de novo brain metastases
  • Median DOR not yet reached; 53% of patients remain on therapy (longest at 23.5 months)
  • No new safety signals; TRAEs > Grade 3 reduced to 28% after dose reduction
  • Company plans to meet with FDA later this year to discuss pivotal development plan
  • Data to be presented at ASCO 2026 on May 30

Financial Impact

Positive Phase 2 data for silevertinib in a large addressable market (EGFR-NCM NSCLC) with potential to become standard of care; no financial figures provided in the release.

pipeline valuemarket opportunity

Risk Factors

  • Phase 2 data is preliminary with small sample size (n=43) and median follow-up of only 11.2 months
  • FDA meeting outcome and pivotal trial design are uncertain
  • Competition from other EGFR TKIs (e.g., osimertinib, amivantamab) in the NCM space
  • Clinical-stage company with no approved products; reliance on successful development and regulatory approval

Market Snapshot

Exchange
Nasdaq
Sector
Biological Products, (No Diagnostic Substances)
Analyst Consensus
87% bullish (15 analysts)

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3299802
5 reports for BDTX
Performance horizon

Track record builds as more directional reports settle.

Filters
Rows
Reports for BDTX — sortable, filterable
Type Now
May 21, 2026
22d ago
8-K
BULLISH ★ 7/10
$2.28 $2.26▼ −0.88%▼ −2.55%$1.75 (−23.25%)
May 21, 2026
22d ago
Press Release
BULLISH ★ 8/10
$2.28 $2.26▼ −0.88%▼ −2.55%$1.75 (−23.25%)
May 7, 2026
5w ago
8-K
NEUTRAL ★ 4/10
$2.72 $2.86▲ +5.15%▲ +3.64%$1.75 (−35.66%)
Apr 21, 2026
7w ago
Press Release
BULLISH ★ 7/10
$3.15 $2.70▼ −14.29%▼ −15.37%$1.75 (−44.44%)
Mar 16, 2026
12w ago
Press Release
MIXED ★ 6/10
$2.23 $2.14▼ −4.04%▼ −1.38%$1.75 (−21.52%)
Showing 5 of 5

US Market Status

Market Closed — Opens Mon (47h 37m)

Subscribe to SecBot

Get Real-Time SEC Filing Intelligence

Comprehensive SEC filing analysis delivered the moment filings hit EDGAR. Sentiment scoring, impact analysis, and actionable insights for every material event.

Try SecBot Free Coming soon: SecBot Pro with alerts, watchlists, and API access