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Life sciences · Phase 1 Trial
ClinicalTrials.gov · October 26, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 1 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
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Registry record from ClinicalTrials.gov (NCT06835569). This is a study registration, not published results. Lead sponsor: Alterome Therapeutics, Inc.. Recruitment status: RECRUITING. Phase: PHASE1. Study type: INTERVENTIONAL. Enrollment: 448 participants (ESTIMATED). Conditions: Cancer, PDAC - Pancreatic Ductal Adenocarcinoma, NSCLC (Non-small Cell Lung Cancer), CRC (Colorectal Cancer), Advanced Solid Tumors. Interventions: DRUG: ALTA3263; DRUG: cetuximab; DRUG: mFOLFOX6; DRUG: Pembrolizumab; DRUG: Pemetrexed + Cisplatin /Carboplatin; DRUG: mFOLFIRINOX; DRUG: GnP; DRUG: Midazolam. Primary outcome measures: Adverse Events , Up to 39 months; Dose Limiting Toxicities , 21 days. Brief summary: The purpose of this study is to characterize the safety and tolerability of ALTA3263 in adults with advanced solid tumors with KRAS mutations.