A Study to Learn About the Study Medicine Called Ponsegromab in Adults With Lung Cancer-Associated Significant Body Weight Loss

Study summary

Study to investigate the effect of ponsegromab on skeletal muscle mass and physical function in adult participants with non-small cell lung cancer associated cachexia.

Ask AI to explain this study

Start here

Key things to know

Main goalSupportive Care

This describes the study’s primary purpose.

What is being studiedponsegromab and placebo

The study team can explain what participation involves.

Who it may be forNon-small cell lung cancer (NSCLC)

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Sep 25, 2026 · Source: ClinicalTrials.gov

Is enrollment open?Not Yet Recruiting

The study is not accepting participants yet.

What kind of study?Phase 1

Interventional

Where is it offered?7 U.S. locations

Locations may change over time.

Who runs it?Pfizer

Study sponsor

Study overview

What this study is about

Purpose: Supportive Care
Study type: Interventional
Phase: Phase 1
Sponsor: Pfizer
Interventions being studied: Drug: ponsegromab; Drug: placebo

Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

Cancer type

Non-small cell lung cancer (NSCLC)→

Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria

Key
Signed Informed Consent
Documented histological or cytologic diagnosis of NSCLC with each of the following: 1. locally advanced, unresectable, stage III disease (according to the 9th edition of the Union for International Cancer Control and American Joint Committee on Cancer lung cancer TNM staging system); and 2. measurable disease at time of screening (assessment per RECIST v1.1); and 3. must have completed platinum-based chemotherapy concurrent with radiation therapy, within 7 to 42 days prior to the randomization; and 4. no evidence of progression of disease following definitive, platinum-based, concurrent chemoradiation therapy; and 5. must be due to receive consolidation immunotherapy with durvalumab for up to 12 months, with the first dose of blinded study intervention to coincide with the first dose of durvalumab +/- 7 days; and 6. absence of actional genomic mutations (eg, EGFR, ALK).
Cachexia defined by Fearon criteria: 1. BMI \<20 kg/m2 and involuntary weight loss of \>2% within 6 months prior to screening; or 2. Involuntary weight loss of \>5% over the past 6 months prior to screening irrespective of BMI
Participant has been evaluated and determined that available anticachexic treatments have either been administered with no positive effect or the participant is not suitable for these treatments.
Participants who are assessed by the investigator to have an ECOG PS ≤1. Key

Reasons someone may not be able to joinExclusion criteria

Current active reversible causes of decreased food intake, as determined by the investigator. These causes may include, but are not limited to: 1. NCI CTCAE Grade 3 or 4 oral mucositis 2. Mechanical obstructions interfering with the participant's ability to eat
Receiving tube feedings or having an ongoing clinical indication for parenteral nutrition (either total or partial) at the time of screening or randomization. Of note: short-term parenteral nutritional support for the management of acute, transient medical indications is allowed if discontinued prior to randomization.
Any prior or current clinical diagnosis of heart failure, irrespective of left ventricular ejection fraction or New York Heart Association classification.
Cachexia caused by reasons other than NSCLC, as determined by the investigator (eg, severe COPD).
Mixed small cell and non-small cell lung cancer histology.
Clinically significant ascites that requires medical intervention or underwent a paracentesis within 4 weeks prior to randomization.
Undergoing major surgery within 4 weeks prior to randomization or planned major surgical procedures during the study.
History of adrenal disorders (e.g. adrenal insufficiency, Cushing syndrome), pituitary adenoma or ectopic ACTH.
Chronic use of systemic corticosteroid.
History of any secondary malignancy in the last 2 years, except for adequately treated basal cell or squamous cell skin cancer or carcinoma in situ.
Symptomatic brain metastasis or leptomeningeal disease.
Any Grade ≥3 pulmonary disease unrelated to underlying malignancy including, but not limited to: 1. Severe asthma requiring systemic corticosteroids within 30 days prior to first dose of study intervention or not well controlled with low-dose inhaled corticosteroids/long-acting beta-2 agonists. 2. Severe chronic obstructive pulmonary disease requiring supplemental oxygen or systemic corticosteroids. 3. Clinically severe and/or Grade 4 pulmonary emboli within 3 months of the first dose of study intervention. Pulmonary emboli in main or lobar pulmonary arteries are also excluded. 4. Any autoimmune or inflammatory disorders with significant pulmonary parenchymal involvement at time of screening (ie, rheumatoid arthritis, Sjögren's syndrome, sarcoidosis, etc).
Renal disease requiring dialysis or eGFR \<30 mL/min/1.73 m².
History of severe liver disease or cirrhosis, unrelated to metastatic cancer. LFT abnormalities at the time of screening; confirmed by a single repeat test if deemed necessary: AST or ALT level ≥ 3 x ULN (\>5 x ULN if liver involvement by the tumor), or total bilirubin level ≥ 1.5 x ULN (For Gilbert's syndrome, direct bilirubin \> ULN is exclusionary).
Left ventricular ejection fraction \<50% on screening echocardiogram (or MUGA scan).

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

Study sites

U.S. locations

Cancer Care Specialists of Illinois-DecaturDecatur, Illinois
Decatur Memorial HospitalDecatur, Illinois
Cancer Care Specialists of Illinois - Cancer Care Center of O'FallonO'Fallon, Illinois
Dallas Cancer SpecialistsGarland, Texas
Houston Cancer Treatment CentersHouston, Texas
Lumi ResearchHouston, Texas
The Universityof Hong Kong-Shenzhen HospitalShenzhen, Guangdong

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Sep 25, 2026. Always confirm current availability with the study team.

View original record ↗