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Controlled Cold Exposure Combined With PD-1/PD-L1 Immunotherapy in Solid Tumors (NIVALIS)

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Summary

NIH ClinicalTrials.gov has registered a single-arm, open-label Phase I exploratory study (NCT07538479) evaluating controlled cold exposure combined with standard PD-1/PD-L1 inhibitor-based therapy in 24 participants with solid malignancies. The primary objectives are to evaluate safety, tolerability, and feasibility of the cold exposure intervention. Secondary objectives include exploring preliminary antitumor activity and effects on brown adipose tissue activation, peripheral immune profiling, circulating cytokines, metabolomics, gut microbiota, and tumor biomarkers.

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What changed

NIH ClinicalTrials.gov registered NCT07538479, a Phase 1 single-arm study examining the safety, tolerability, and feasibility of adding controlled cold exposure to standard PD-1/PD-L1 inhibitor-based therapy in participants with solid malignancies. The cold acclimation phase involves exposure to approximately 20C for 8 hours and 18C for 10 hours, followed by formal intervention with 18C exposure for 12 hours per day over 7 consecutive days concurrent with immunotherapy cycles.

Affected parties include patients with solid malignancies eligible for enrollment and clinical investigators conducting Phase 1 oncology trials. This study registration does not create compliance obligations for sponsors, manufacturers, or healthcare providers beyond standard clinical trial conduct requirements. The trial is registered under ClinicalTrials.gov identifier NCT07538479.

Archived snapshot

Apr 21, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

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Controlled Cold Exposure Combined With PD-1/PD-L1 Immunotherapy in Solid Tumors (NIVALIS)

Phase 1 NCT07538479 Kind: PHASE1 Apr 20, 2026

Abstract

This is a single-center, prospective, single-arm, open-label phase I exploratory study that plans to enroll 24 participants with solid malignancies. All participants will receive controlled cold exposure in addition to standard PD-1/PD-L1 inhibitor monotherapy or PD-1/PD-L1 inhibitor-based standard combination therapy. A 2-day cold acclimation phase will precede formal intervention, consisting of approximately 20°C exposure for 8 hours on Day -2 and approximately 18°C exposure for 10 hours on Day -1. The first combination cycle begins on Day 1 concurrently with PD-1/PD-L1-based treatment, with exposure to an 18°C temperature-controlled hospital room for 12 hours per day for 7 consecutive days. If tolerated, cold exposure may be repeated in subsequent PD-1/PD-L1 treatment cycles. The primary objective is to evaluate safety, tolerability, and feasibility. Secondary objectives are to explore preliminary antitumor activity and the effects on brown adipose tissue activation, peripheral immune profiling, circulating cytokines, metabolomics, gut microbiota, patient-reported outcomes, and tumor immune/metabolic biomarkers when paired tumor tissue is available.

Conditions: Solid Tumors, Solid Malignancies, Cold Exposure, Immunotherapy

Interventions: Controlled Cold Exposure, Investigator-Selected Standard PD-1/PD-L1 Inhibitor-Based Therapy

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Last updated

Classification

Agency
NIH
Published
April 20th, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Patients Clinical investigators
Industry sector
6211 Healthcare Providers
Activity scope
Immunotherapy administration Phase 1 clinical trial Cold exposure protocol
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Public Health Pharmaceuticals

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