GB18 Injection Phase I Tumor Cachexia Trial
Summary
The National Library of Medicine registered a Phase I clinical trial (NCT07519564) evaluating GB18 Injection in approximately 24 adults with tumor cachexia. The single-center, non-randomized study will assess safety, tolerability, and pharmacokinetics with an estimated completion date of December 2025.
Healthcare providers and patients seeking experimental treatment options for cancer-related muscle wasting may reference this trial for enrollment eligibility. Sponsors conducting similar cachexia research should ensure their studies are similarly registered to maintain transparency and regulatory compliance.
What changed
NLM registered a new Phase I clinical trial on ClinicalTrials.gov for GB18 Injection as a treatment for tumor cachexia, a wasting syndrome associated with cancer. The trial is classified as Phase I (early-stage safety evaluation), non-randomized, and expects to enroll approximately 24 adult participants at a single US site.
Affected parties should note this trial represents an early-stage drug development milestone. Healthcare providers treating cachexia patients may consider referring suitable candidates. Pharmaceutical researchers should ensure their cachexia programs maintain current registrations. This registration has no immediate compliance obligations but establishes the trial's public record for regulatory transparency.
What to do next
- Monitor ClinicalTrials.gov for updates on enrollment status
Archived snapshot
Apr 11, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
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