A Study of NKT2152, a HIF2α Inhibitor, in Patients With Advanced Clear Cell Renal Cell Carcinoma
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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.
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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
- Enrollment
- 120 participants
Conditions and interventions
Conditions
- ccRCC
- Clear Cell Renal Cell Carcinoma
- Kidney Cancer
- Kidney Neoplasms
- Renal Cancer
- Renal Neoplasms
- Recurrent Renal Cell Carcinoma
- Metastatic Renal Cell Carcinoma
- Refractory Renal Cell Carcinoma
- Advanced Renal Cell Carcinoma
- Hypoxia
- Renal Cell Carcinoma
- Hypoxia Inducible Factor (HIF)
- HIF2α Inhibitor
- Hypoxia Inducible Factor 2 Alpha (HIF-2 Alpha)
- Hypoxia Inducible Factor 2α (HIF-2α)
- Clear Cell
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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