Sutro Biopharma (NASDAQ:STRO) announces
updated interim data regarding safety and anti-tumor activity results
in heavily pre-treated patients with ovarian cancer from Phase 1
clinical trial evaluating its folate receptor alpha (FolRα) antibody
drug-conjugate STRO-002.
75% of patients have initial post-baseline scans showing stable disease or a partial response.
13 patients had a ≥50% reduction or normalization
of CA-125, including six confirmed responses, six unconfirmed responses
and one prolonged CA-125 normalization.
100% of evaluable patients have achieved stable disease or a confirmed partial response.
STRO-002 was generally well-tolerated. 89% of adverse events reported were grade 1 or 2.
A dose expansion phase of this trial is planned to
commence in H2. Although maximum tolerated dose has not been reached,
Sutro is continuing to actively explore the 5.2 mpk to 6.0 mpk dose
levels as it seeks to determine the recommended Phase 2 dose.
Sutro will host a conference call today at 8 a.m. EDT to discuss the STRO-002 data.
https://seekingalpha.com/news/3564519-sutro-biopharma-reports-encouraging-data-from-early-stage-strominus-002-study
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