A Clinical Trial of PF-08046037 Alone or With Sasanlimab in Patients With Advanced or Metastatic … (NCT06974734) | Clinical Trial Compass
TerminatedPhase 1
A Clinical Trial of PF-08046037 Alone or With Sasanlimab in Patients With Advanced or Metastatic Malignancies
Stopped: The trial was terminated for strategic business reasons; the decision was not based on any safety and/or efficacy concerns
United States, Puerto Rico8 participantsStarted 2025-05-06
Plain-language summary
The purpose of this study is to learn about the safety and the effects of PF-08046037 alone or with sasanlimab for the treatment of certain advanced or metastatic malignancies.
This study is seeking participants who:
* have advanced or metastatic non-small cell lung cancer (NSCLC), head and neck squamous cell carcinoma (HNSCC), melanoma, or pancreatic ductal adenocarcinoma (PDAC);
* are able to provide tumor tissue samples;
* have measurable disease. All participants will receive while at the clinic PF-08046037 alone as an intravenous (IV) infusion (given directly into a vein) or with sasanlimab as a subcutaneous (SQ) injection (given under the skin) once every 3 weeks.
Participants will continue to take the study drug(s) until their cancer is no longer responding or if the patient cannot safely take them. The study team will monitor how each participant is doing with the study treatment during regular visits at the study clinic.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
This study is seeking participants who have the following tumor types and can provide tumor tissue samples as per below.
1. Tumor types
* Monotherapy Dose Escalation (Part 1a) and Optimization (Part 2a) cohorts
* Advanced or metastatic NSCLC, HNSCC, melanoma, or PDAC
* Must have progressive disease following at least 1 prior approved systemic therapy
* Monotherapy Dose Expansion (Part 3a)
• Advanced or metastatic NSCLC or PDAC
* Combination Safety Evaluation (Part 1b) and Dose Optimization (Part 2b)
* Advanced or metastatic NSCLC or HNSCC
* May be either a) not received prior immunotherapy for the tumor type OR b) relapse/ refractory after prior immunotherapy
* Combination Dose Expansion (Part 3b)
* Unresectable locally advanced or metastatic HNSCC or NSCLC
* Must not have received prior systemic cytotoxic therapy in the locally advanced or metastatic setting (first-line setting)
* Must be treatment naïve to any immunotherapy
* NSCLC must have PD-L1 expression TPS \>=50%
* HNSCC must have PD-L1 expression CPS \>=1
2. Tissue requirement
* Part 1 at lower doses: sufficient archival tissue collected within 12 months of enrollment for submission to central laboratory
* Part 1 at higher doses: de novo baseline tumor biopsy or archival tissue within 12 months of enrollment
* Part 1 backfill: de novo baseline and on-treatment tumor biopsies are required
* Part 2 and 3: de novo baseline or archival tissu…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Number of participants with adverse events (AEs)
Timeframe: Through 30-37 days after the last study treatment, up to approximately 2 years
2
Number of participants with laboratory abnormalities
Timeframe: Through 30-37 days after the last study treatment, up to approximately 2 years
3
Number of dose modifications due to AEs
Timeframe: Through end of treatment up to approximately 2 years
4
Number of participants with dose-limiting toxicities (DLTs)