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NCT07405086 · ClinicalTrials.gov registry record · Phase 4
Morning Versus Afternoon Administration of Immunotherapy for the Treatment of Advanced or Metastatic Solid Tumors, The Knight SHIFT Study
A Phase 4 study, sponsored by OHSU Knight Cancer Institute.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 160
- Enrollment target
NCT07405086: Recruiting Phase 4 study, sponsored by OHSU Knight Cancer Institute.
NCT07405086 is a Phase 4 study that is actively recruiting participants, run by OHSU Knight Cancer Institute. The registered enrollment target is 160 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (69% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07405086, a Phase 4 study, is actively recruiting participants, sponsored by OHSU Knight Cancer Institute.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 160 participants
- Enrollment target
Study Summary
This phase IV trial is evaluating whether morning versus afternoon administration of standard of care immunotherapy impacts its effectiveness in treating patients with solid tumors that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic). Immunotherapy with monoclonal antibodies may help the body's immune system attack the cancer and may interfere with the ability of tumor cells to grow and spread. Circadian rhythm refers to the internal biological clock in which various processes in the body, including immune cell activity, are controlled by the time of day. Exactly how this works is not fully understood, and the researchers want to see if circadian rhythm control of the immune system can influence response to immunotherapy based on whether it is given in the morning (before 11:00 am) or afternoon (12:00pm). The time of day that immunotherapy is given (morning versus afternoon) may impact the effectiveness in treating patients with advanced or metastatic solid tumors.
Primary Outcome
The associated 95% confidence interval (CI) for each treatment group will be estimated using the Kaplan-Meier method. The stratified hazard ratio (HR) and its 95% CI will be estimated using a Cox proportional-hazard model with treatment group as the independent variable and stratified by the same randomization stratification factors as were used for the log-rank test.
Interventions
- PROCEDURE Biospecimen Collection
- DRUG Immune Checkpoint Inhibitor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 160 participants |
| Start Date | 2026-06-08 |
| Est. Completion | 2028-12-31 |
| Phase | Phase 4 |
What NCT07405086 shows while recruiting
NCT07405086 is an interventional study that assigns participants to a tested intervention. The registered 160 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (69% lower).
The record links to 0 conditions, and to 2 interventions - of which Biospecimen Collection is the first listed.
NCT07405086 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07405086 about?
NCT07405086 is a clinical study titled "Morning Versus Afternoon Administration of Immunotherapy for the Treatment of Advanced or Metastatic Solid Tumors, The Knight SHIFT Study". This phase IV trial is evaluating whether morning versus afternoon administration of standard of care immunotherapy impacts its effectiveness in treating patients with solid tumors that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced)...
What is the current status of trial NCT07405086?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 160 participants. The study started on 2026-06-08. Estimated completion is 2028-12-31.
What interventions are being tested in trial NCT07405086?
The interventions under investigation include: Biospecimen Collection (PROCEDURE), Immune Checkpoint Inhibitor (DRUG).
Who is sponsoring clinical trial NCT07405086?
This trial is sponsored by OHSU Knight Cancer Institute, which has 211 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07405086's enrollment target sits among peer trials
160 507th of 2000 higher than 1,485 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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