PF-08098488 for Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new medicine, PF-08098488, for individuals with advanced cancers such as non-small cell lung cancer, pancreatic cancer, stomach/gastroesophageal junction cancer, or esophageal cancer. Researchers focus on the medicine's safety and potential effectiveness by experimenting with different doses and schedules. Participants qualify if their cancer has progressed despite previous treatments. All participants will receive the medicine through an IV infusion and will be closely monitored at the study clinic. Regular check-ups, including scans and blood tests, will track their progress. As a Phase 1 trial, this research aims to understand how the treatment works in people, offering participants the opportunity to be among the first to receive this new treatment.
Is there any evidence suggesting that PF-08098488 is likely to be safe for humans?
Research has shown that PF-08098488 is currently being tested for safety in people with advanced cancers. As this treatment is new and the study is in its early stages, detailed safety information remains limited. However, early trials are designed to closely monitor how patients respond to the drug. Participants receive careful observation, especially after the first treatment, to identify any side effects or issues. This process helps researchers determine the safest dose for future studies. While specific safety results for PF-08098488 are not yet available, the primary goal at this stage is to ensure the treatment's safety for patients.12345
Why do researchers think this study treatment might be promising?
PF-08098488 is unique because it targets cancer cells differently from standard chemotherapy and immunotherapy options. While traditional treatments often attack both healthy and cancerous cells, PF-08098488 aims to selectively target tumor cells, potentially reducing side effects. Researchers are excited about its novel mechanism of action, which could offer a more precise treatment approach and improve patient outcomes.
What evidence suggests that PF-08098488 might be an effective treatment for advanced solid tumors?
Research has shown that PF-08098488 is under study as a treatment for advanced cancers, including non-small cell lung cancer and pancreatic cancer. Participants in this trial will join different treatment arms: Part 1 Dose Escalation, Part 2 Dose Expansion, and Part 2 Dose Optimization, to evaluate various doses and schedules of PF-08098488. Although information on its effectiveness in people is limited, this treatment targets specific cancer pathways, potentially slowing or stopping cancer growth. Early research on similar treatments has demonstrated that targeting these pathways can sometimes lead to better outcomes, such as longer survival or smaller tumors. The goal is to determine if PF-08098488 can achieve similar results in these challenging cancers. More information is needed to confirm its effects, but its mechanism offers hope for effectiveness.678910
Who Is on the Research Team?
Pfizer CT.gov Call Center
Principal Investigator
Pfizer
Are You a Good Fit for This Trial?
This trial is for adults with advanced cancers such as non-small cell lung, pancreatic, stomach, gastroesophageal junction, or esophageal cancer. Participants must have tried at least one previous treatment and have cancer that has grown or stopped responding to other therapies.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive PF-08098488 as an IV infusion with different dose levels and dosing schedules to find the safest and most effective dose
Follow-up
Participants are monitored for safety and effectiveness after treatment, with a follow-up visit about 1 month later and health checks every 12 weeks
What Are the Treatments Tested in This Trial?
Interventions
- PF-08098488
Trial Overview
The study is testing a new medicine called PF-08098488 given by IV infusion in people with certain advanced cancers. All participants receive the drug while researchers test different doses to find the safest and most effective amount.
How Is the Trial Designed?
3
Treatment groups
Experimental Treatment
Participants will be assigned to one of two dosing regimens deemed to be safe in Part 1
Participants in tumor-specific groups will receive 1 dosing regimen deemed to be safe in Part 1
Different groups of participants will receive different doses and/or schedules of the study drug
Find a Clinic Near You
Who Is Running the Clinical Trial?
Pfizer
Lead Sponsor
Albert Bourla
Pfizer
Chief Executive Officer since 2019
PhD in Biotechnology of Reproduction, Aristotle University of Thessaloniki
Patrizia Cavazzoni
Pfizer
Chief Medical Officer
MD from McGill University
Citations
Examining the Effectiveness of Electronic Patient-Reported ...
The meta-analysis showed an improvement in HRQOL at 3 months, measured by the Functional Assessment of Cancer Therapy–General (SMD 0.29, 95% CI ...
Evaluation of the Use of Cancer Registry Data for ... - PubMed
The findings of this study suggest that comparative effectiveness research using cancer registry data often produces survival outcomes ...
A Study to Learn About the Study Medicine Called PF ...
PF-08098488 is being studied as a possible treatment for certain types of cancer. These include non-small cell lung cancer, pancreatic cancer, ...
4.
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oncologynewscentral.com/oncology/positive-cancer-trials-with-surrogate-endpoints-rarely-improve-survival-quality-of-life“Positive” Cancer Trials With Surrogate Endpoints Rarely ...
A study of nearly 800 phase 3 trials presented at ASCO 2025 found that surrogate endpoints rarely result in improved quality of life or ...
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Designed to assess physicians' use of screening modalities, therapies, new technologies, and other factors that may influence the cancer burden ...
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trial.medpath.com/clinical-trial/4f12a77fbc5d7f2a/jprn-jrct2031200246-phase-1-pf-07248144-solid-tumorsStudy of PF-07248144 in Advanced or... | Clinical Trial
Study to evaluate the effectiveness, safety and tolerability of nivolumab in subjects with advanced liver cancer.MedDRA version: 19.1Level ...
A Study of PF-08046050 (SGN-CEACAM5C) in Adults ...
PF-08046050 is a type of antibody-drug conjugate or ADC. ADCs are designed to stick to cancer cells and kill them. They may also stick to some normal cells.
8.
ctv.veeva.com
ctv.veeva.com/study/a-study-to-learn-about-the-study-medicine-called-pf-08032562-in-people-with-advanced-or-metastatic-sA Study to Learn About the Study Medicine Called PF ...
The purpose of this study is to learn about the safety and effects of the study medicine when given alone or together with other anti-cancer ...
Efficacy and safety profile of combining vandetanib with ...
Efficacy and safety profile of combining vandetanib with chemotherapy in patients with advanced non-small cell lung cancer: a meta-analysis.
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trial.medpath.com/clinical-trial/16970152f3d2bee2/ctis2022-502369-10-00-sacituzumab-govitecan-triple-negative-breast-cancerSafety and efficacy analysis of an... | Clinical Trial
ISIdE: Open label, multicentric, single-arm phase IIIB trial to evaluate the safety and efficacy of sacituzumab govitecan in triple negative ...
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