Evidence map›Paper›PMID 38500292›Full record

Trial reportJournal of cachexia, sarcopenia and muscle2024

Phase 2 study of the efficacy and safety of ponsegromab in patients with cancer cachexia: PROACC-1 study design.

John D Groarke, Jeffrey Crawford, Susie M Collins, Shannon L Lubaczewski, Danna M Breen, Magdalena A Harrington, Ira Jacobs, Ruolun Qiu, James Revkin, Michelle I Rossulek and 1 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal of cachexia, sarcopenia and muscle, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05546476 (A PHASE 2, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO INVESTIGATE THE EFFICACY, SAFETY AND TOLERABILITY OF PONSEGROMAB IN PATIENTS WITH CANCER, CACHEXIA, AND ELEVATED CONCENTRATIONS OF GDF-15, FOLLOWED BY AN OPTIONAL OPEN-LABEL TREATMENT PERIOD), which is not on this map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
16.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05546476 phase2completednot on this map

A phase 2, randomized, double-blind, placebo-controlled study to investigate the efficacy, safety and tolerability of ponsegromab in patients with cancer, cachexia, and elevated concentrations of gdf-15, followed by an optional open-label treatment period (proacc -1)

TypeinterventionalSponsorPfizerRan2022 to 2025Enrolled187ConditionsNon-small Cell Lung Cancer, Pancreatic Cancer, Colorectal Cancer, Loss of AppetiteArmsponsegromab, Placebo for ponsegromab
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

John D GroarkeInternal Medicine Research Unit, Pfizer Inc, Cambridge, MA, USA.
Jeffrey CrawfordDuke Cancer Institute, Duke University Medical Center, Durham, NC, USA.
Susie M CollinsGlobal Biometrics and Data Management, Pfizer R&D UK Ltd, Sandwich, Kent, UK.
Shannon L LubaczewskiEarly Clinical Development and Biomedicine Artificial Intelligence, Pfizer Inc, Collegeville, PA, USA.
Danna M BreenInternal Medicine Research Unit, Pfizer Inc, Cambridge, MA, USA.
Magdalena A HarringtonGlobal Access and Value, Pfizer Inc, Cambridge, MA, USA.
Ira JacobsGlobal Product Development, Pfizer Inc, New York, NY, USA.
Ruolun QiuClinical Pharmacology, Pfizer Inc, Cambridge, MA, USA.
James RevkinInternal Medicine Research Unit, Pfizer Inc, Cambridge, MA, USA.
Michelle I RossulekInternal Medicine Research Unit, Pfizer Inc, Cambridge, MA, USA.
Aditi R SaxenaInternal Medicine Research Unit, Pfizer Inc, Cambridge, MA, USA.
Pfizer (United States) · USDuke Medical Center · USPfizer (United Kingdom) · GB

Funding

Pfizer
6 · The paper itself

Abstract

backgroundCancer cachexia is a multifactorial metabolic wasting syndrome characterized by anorexia, unintentional loss of weight involving both skeletal muscle and adipose tissues, progressive functional impairment and reduced survival. Therapeutic strategies for this serious condition are very limited. Growth differentiation factor 15 (GDF-15) is a cytokine that is implicated in cancer cachexia and may represent both a biomarker of cancer cachexia and a potential therapeutic target. Ponsegromab is a potent and selective humanized monoclonal antibody that inhibits GDF-15-mediated signalling. Preclinical and preliminary phase 1 data suggest that ponsegromab-mediated inactivation of circulating GDF-15 may lead to improvement in key characteristics of cachexia. The primary objective of this phase 2 study is to assess the effect of ponsegromab on body weight in patients with cancer, cachexia and elevated GDF-15 concentrations. Secondary objectives include assessing physical activity, physical function, actigraphy, appetite, nausea and vomiting, fatigue and safety. Exploratory objectives include evaluating pharmacokinetics, pharmacodynamics, immunogenicity, lumbar skeletal muscle index and Response Evaluation Criteria in Solid Tumors.

methodsApproximately 168 adults with non-small-cell lung, pancreatic or colorectal cancers who have cachexia and elevated GDF-15 concentrations will be randomized in a double-blind, placebo-controlled study (NCT05546476). Participants meeting eligibility criteria will be randomized 1:1:1:1 to one of three dose groups of ponsegromab (100, 200 or 400 mg) or matching placebo administered subcutaneously every 4 weeks for an initial 12-week treatment period. This is followed by optional open-label treatment with ponsegromab of 400 mg administered every 4 weeks for up to 1 year. The primary endpoint is mean change from baseline in body weight at Week 12. A mixed model for repeated measures followed by a Bayesian E PERSPECTIVE: Cancer-related cachexia is an area of significant unmet medical need. This study will support the clinical development of ponsegromab as a novel inhibitor of GDF-15, which may ameliorate key pathologies of cancer cachexia to improve patient symptoms, functionality and quality of life.

trial registrationClinicalTrials.gov ID: NCT05546476.

Indexed as

CachexiaNeoplasmsAdultAntibodies, Monoclonal, HumanizedFemaleGrowth Differentiation Factor 15HumansMaleAntibodies, Monoclonal, HumanizedGrowth Differentiation Factor 15cachexiacancerGDF‐15ponsegromabweight loss

Identifiers

PMID38500292
PMCPMC11154777
OpenAlexW4392965707

What OpenQuestion holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.