CI

At a glance

ClinicalIndex Comparison Record
Phase 1Unknown· 110 target
Drug / intervention
XKH002 Injectiondrug
Likely dose
XKH002 Injection 240 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06196762
NCT06196762Phase 1Unknown

A Phase 1, First-in-human (FIH),Dose-escalation and Dose-expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antitumor Activity of XKH002 in Patients With Advanced or Metastatic Solid Tumors

Zhejiang Kanova Biopharmaceutical Co., LTD·interventional·Posted Jan 9, 2024·Updated Oct 10, 2024

In Brief

A Phase 1 clinical trial evaluating XKH002 Injection for Advanced or Metastatic Solid Tumors. Targeting 110 participants across 1 site.

Detailed Summary

This is a Phase 1, first-in-human (FIH), open-label, multicenter, dose-escalation and dose-expansion study to evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of XKH002 in patients with advanced or metastatic solid tumors.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 1UnknownOverdue
202420252026
First PostedJan 9, 2024
Enrollment StartNov 27, 2023
Primary CompletionDec 1, 2025
Study CompletionApr 1, 2026
TodayJul 1, 2026
Enrollment to primary: 2.0 yearsPosted 2.5 years ago

Interventions

XKH002 Injectiondrug

240 mg/4 mL/vial(60 mg/mL)