OncoMatch/Clinical Trials/NCT06266299
A Study of KK2269 in Adult Participants With Solid Tumors
Is NCT06266299 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including KK2269 and Docetaxel for advanced solid tumor.
Treatment: KK2269 · Docetaxel — This is a first-in-human study of KK2269. Part 1 and Part 2 will be conducted as a multicenter, open-label, non-randomized, dose-escalation study. Participants with advanced or metastatic solid tumors for which no standard therapy is available will be enrolled in Part 1. In Part 1, the primary objective is to assess the safety and tolerability of KK2269. In Part 2, only participants with gastric adenocarcinoma, GEJ adenocarcinoma, esophageal adenocarcinoma, or NSCLC who have experienced at least one systemic therapy will be enrolled. In Part 2, the primary objective is to assess the safety and tolerability of KK2269 in combination with docetaxel and to determine the recommended dose(s) and dose interval(s) of KK2269 in combination with docetaxel for subsequent studies. In both Part 1 and Part 2, participants who refuse to undergo standard therapy are also eligible.
Check if I qualifyExtracted eligibility criteria
Cancer type
Tumor Agnostic
Gastric Cancer
Esophageal Carcinoma
Small Cell Lung Cancer
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Cannot have received: docetaxel (docetaxel)
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Mayo Clinic Arizona · Scottsdale, Arizona
- City Of Hope National Medical Center · Duarte, California
- Hoag Memorial Hospital Presbyterian · Newport Beach, California
- Mayo Clinic Jacksonville · Jacksonville, Florida
- Washington University · St Louis, Missouri
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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