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Terminated Phase 1Phase 2 Interventional

A Study of NKT2152, a HIF2α Inhibitor, in Patients With Advanced Clear Cell Renal Cell Carcinoma

ClinicalTrials.gov ID: NCT05119335

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT05119335. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 13, 2026, 2:06 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 1/2 Open Label Dose-escalation and Expansion Trial of NKT2152 an Orally Administered HIF2α Inhibitor to Investigate Safety Pharmacokinetics Pharmacodynamics and Clinical Activity in Patients With Advanced Clear Cell Renal Cell Carcinoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of the Phase 1 portion is to identify the maximum tolerated dose (MTD) and/or the recommended doses for expansion (RDEs) of NKT2152. The Phase 2 portion will evaluate the efficacy of NKT2152 in ccRCC.

Study identification

NCT ID
NCT05119335
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
NiKang Therapeutics, Inc.
Industry
Enrollment
120 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 26, 2021 (Actual)
Primary completion
Aug 22, 2025 (Actual)
Completion
Sep 30, 2025 (Actual)
Last update posted
Nov 12, 2025

2021 – 2025

United States locations

U.S. sites
13
U.S. states
13
U.S. cities
13
Facility City State ZIP Site status
HonorHealth Scottsdale Arizona 85258 —
UCLA Los Angeles California 90095 —
Sarah Cannon Research Institute Denver Colorado 80218 —
Emory University Atlanta Georgia 30322 —
Indiana University Simon Comprehensive Cancer Center Indianapolis Indiana 46202 —
University of Iowa Iowa City Iowa 52242 —
National Cancer Institute Bethesda Maryland 20892-9760 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
Nebraska Cancer Specialists Omaha Nebraska 68130 —
University of Oklahoma Oklahoma City Oklahoma 73117 —
Oregon Health and Science University Portland Oregon 97239 —
MD Anderson Cancer Center Houston Texas 77030 —
Seattle Cancer Care Alliance Seattle Washington 98109 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05119335, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 12, 2025 · Synced Nov 13, 2026

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