TRDA Entrada Therapeutics, Inc.

NEUTRAL Impact: 4/10 PRESS-RELEASE
Horizon weeks Filed Jun 2, 2026 Processed 12d 21h ago Wire GlobeNewswire
Press release: fda
Latest settled — T+1d
TRDA ▼ -0.90% at T+1d
NEUTRAL call ✗ call lost -0.90% · α vs SPY -0.18% · entry $6.64 → $6.58
Next anchor: T+5d due 6d ago
Last close $6.46 (close Jun 12) · -2.71% from $6.64 entry
Entry anchored
Jun 2, 2026
via day open
T+1d
-0.90%
call -0.90% · α -0.18%
$6.58
settled 12d ago
T+5d
call — · α —
due 6d ago
T+20d
call — · α —
in 16d
T+60d
call — · α —
in 2mo

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Executive Summary

Entrada Therapeutics announced that an independent DMC recommended dose escalation to 10 mg/kg in Cohort 2 of the ELEVATE-45-201 Phase 1/2 study for ENTR-601-45 in Duchenne muscular dystrophy (exon 45). The company remains on track to report Cohort 1 safety, PK, and dystrophin data in mid-2026, with Cohort 2 and 3 data to follow. This is a routine clinical progress update with no new efficacy data released, making the near-term impact neutral.

Actionable Insight

Monitor mid-2026 for Cohort 1 dystrophin data, which will be the first efficacy readout for ENTR-601-45. Positive dystrophin expression could drive significant upside for this single-asset-stage biotech; negative or ambiguous data would be highly bearish. Until then, no near-term catalyst.

Key Facts

  • DMC recommended initiation of Cohort 2 at 10 mg/kg (up from 5 mg/kg in Cohort 1) after reviewing safety and PK data from 8 participants.
  • Company on track to report Cohort 1 data (safety, early PK, dystrophin) in mid-2026.
  • ELEVATE-45-201 is a Phase 1/2 MAD study of ENTR-601-45 for DMD patients amenable to exon 45 skipping.
  • Dosing regimen is once every six weeks; planned doses across three cohorts range from 5 mg/kg to 15 mg/kg.
  • No financial data, revenue, or earnings were disclosed in the press release.

Financial Impact

No financial figures disclosed; pre-revenue clinical-stage biotech.

Risk Factors

  • Cohort 1 data (mid-2026) may show insufficient dystrophin expression or safety signals, leading to program termination.
  • DMD exon 45 space is competitive (Sarepta's Casimersen already approved); differentiation on efficacy or dosing frequency is unproven.
  • Pre-revenue company with limited cash runway — future dilution risk for ongoing trials.

Market Snapshot

Exchange
Nasdaq
Sector
Pharmaceutical Preparations
Analyst Consensus
93% bullish (14 analysts)

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3304981
8 reports for TRDA
Performance horizon

Track record builds as more directional reports settle.

Filters
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Reports for TRDA — sortable, filterable
Type Now
Jun 10, 2026
4d ago
8-K
NEUTRAL ★ 2/10
$5.96 awaiting T+1awaiting T+1$6.46 (+8.39%)
Jun 2, 2026
12d ago
Press Release
NEUTRAL ★ 4/10
$6.64 $6.58▼ −0.90%▼ −0.18%$6.46 (−2.71%)
May 7, 2026
5w ago
Press Release
MIXED ★ 6/10
$6.85 $6.84▼ −0.15%▼ −0.98%$6.46 (−5.69%)
May 4, 2026
5w ago
144
NEUTRAL ★ 2/10
$15.75 $16.03▲ +1.78%▲ +0.39%$6.46 (−58.98%)
May 4, 2026
6w ago
Insider Cluster
BEARISH ★ 5/10
$15.79 $15.75▲ +0.25%▲ +1.05%$6.46 (+59.09%)
Apr 24, 2026
7w ago
DEFA14A
NEUTRAL ★ 3/10
$12.63 $12.96▲ +2.61%▲ +2.45%$6.46 (−48.85%)
Mar 4, 2026
14w ago
Insider Cluster
NEUTRAL ★ 3/10
$12.50 $11.62▼ −7.04%▼ −6.47%$6.46 (−48.32%)
Feb 26, 2026
15w ago
8-K
BEARISH ★ 6/10
$12.79 $11.93▲ +6.72%▲ +6.27%$6.46 (+49.49%)
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