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ePoster Display

1696TiP - Phase Ib study to assess the effect of PF-06946860 on appetite following subcutaneous administration in patients with anorexia and advanced cancer

Date

16 Sep 2021

Session

ePoster Display

Topics

Supportive Care and Symptom Management;  Clinical Research

Tumour Site

Presenters

Eric Roeland

Citation

Annals of Oncology (2021) 32 (suppl_5): S1175-S1198. 10.1016/annonc/annonc714

Authors

E.J. Roeland1, S. Yennu2, E. Del Fabbro3, C. Buckeridge4, K.M. Thayer5, S.M. Collins6, S.L. Lubaczewski7, E.Q. Wang8, R.A. Calle4

Author affiliations

  • 1 Knight Cancer Institute, Oregon Health and Sciences University, 97239 - Portland/US
  • 2 Palliative, Rehabilitation And Integrative Medicine, University of Texas MD Anderson Cancer Center, 77030 - Houston/US
  • 3 Department Of Internal Medicine, Virginia Commonwealth University, 23298 - Richmond/US
  • 4 Internal Medicine Research Unit, Pfizer Worldwide Research and Development, 02139 - Cambridge/US
  • 5 Clinical Development And Operations, Pfizer Inc, 10017 - New York/US
  • 6 Early Clinical Development, Pfizer R&D UK Ltd, CB21 6GP - Sandwich, Kent/GB
  • 7 Early Clinical Development, Pfizer Inc, 19426 - Collegeville/US
  • 8 Early Clinical Development, Clinical Pharmacology, Pfizer Inc, 10017 - New York/US

Resources

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Abstract 1696TiP

Background

Cachexia is a hypermetabolic multifactorial syndrome characterized by anorexia and loss of weight and skeletal muscle, leading to fatigue, functional impairment, increased treatment-related toxicity, poor quality of life, and reduced survival. Anorexia is a central component of the cachectic phenotype and may be primarily mediated by growth differentiation factor 15 (GDF-15). Neutralization of GDF-15 may improve anorexia and other cancer cachexia-related clinical outcomes. PF-06946860 is a highly potent and selective humanized monoclonal antibody directed against GDF-15. The primary objective of this study (NCT04803305) is to assess the effect of repeated subcutaneous (SC) administration of PF-06946860 on appetite in participants with advanced cancer and elevated circulating GDF-15 concentrations. Secondary objectives include assessing fatigue and safety. Exploratory objectives include evaluating body weight, pharmacokinetics, pharmacodynamics, and immunogenicity.

Trial design

The study will be conducted in 2 parts in approximately 40 adult male or female participants with incurable cancer, including non-small cell lung, pancreatic, colorectal, prostate, breast, and ovarian cancers, as well as anorexia and elevated concentrations of GDF-15. The initial 6-week treatment period will be a randomized, double-blind, placebo-controlled, parallel-group study wherein participants who meet entry criteria will be randomized (2:1) to PF-06946860 or placebo, administered SC every 3 weeks. This period will be followed by an optional open-label treatment with PF-06946860 for up to 18 weeks. The primary outcome measure is change from baseline for the patient-reported 7-day recall Cancer-Related Cachexia Symptom Assessment-Appetite score at Week 4. Secondary outcome measures include patient-reported fatigue (Fatigue score from the Cancer-Related Cachexia Symptom Assessment), adverse events, and laboratory abnormalities. The study is currently recruiting participants in the US, with planned sites in Canada.

Clinical trial identification

NCT04803305.

Editorial acknowledgement

Medical writing support was provided by Diane Hoffman, PhD, of Engage Scientific Solutions, and was funded by Pfizer.

Legal entity responsible for the study

Pfizer.

Funding

Pfizer.

Disclosure

E.J. Roeland: Financial Interests, Institutional, Advisory Role, Honoraria: Prime Oncology; Financial Interests, Institutional, Advisory Role: Pfizer; Financial Interests, Institutional, Advisory Role: Helsinn Therapeutics; Financial Interests, Institutional, Advisory Role: Napo Pharmaceuticals; Financial Interests, Institutional, Advisory Role: Heron Therapeutics; Financial Interests, Institutional, Advisory Role: Asahi Kasei; Financial Interests, Institutional, Other, Data Monitoring Committee: Oragenics Inc; Financial Interests, Institutional, Other, Data Monitoring Committee: Galera Pharmaceuticals; Financial Interests, Institutional, Other, Data Monitoring Committee: Enzychem Lifesciences; Financial Interests, Institutional, Expert Testimony: Regents of University of California. S. Yennu: Financial Interests, Institutional, Advisory Role: Pfizer; Financial Interests, Institutional, Funding, Research: Genentech; Financial Interests, Institutional, Funding, Research: Helsinn Healthcare. E. Del Fabbro: Financial Interests, Institutional, Advisory Role: Pfizer; Financial Interests, Institutional, Advisory Role: Helsinn Therapeutics. C. Buckeridge: Financial Interests, Institutional, Full or part-time Employment: Pfizer; Financial Interests, Institutional, Stocks/Shares: Pfizer. K.M. Thayer: Financial Interests, Institutional, Full or part-time Employment: Pfizer; Financial Interests, Institutional, Stocks/Shares: Pfizer. S.M. Collins: Financial Interests, Institutional, Full or part-time Employment: Pfizer; Financial Interests, Institutional, Stocks/Shares: Pfizer. S.L. Lubaczewski: Financial Interests, Institutional, Full or part-time Employment: Pfizer; Financial Interests, Institutional, Stocks/Shares: Pfizer. E.Q. Wang: Financial Interests, Institutional, Full or part-time Employment: Pfizer; Financial Interests, Institutional, Stocks/Shares: Pfizer. R.A. Calle: Financial Interests, Institutional, Full or part-time Employment: Pfizer; Financial Interests, Institutional, Stocks/Shares: Pfizer.

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