CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 18 enrolled
Drug / intervention
PF-06946860 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04803305
NCT04803305Phase 1Completed

A 6-WEEK, RANDOMIZED, DOUBLE-BLIND, SPONSOR-OPEN STUDY TO ASSESS THE EFFECT OF REPEATED SUBCUTANEOUS ADMINISTRATION OF PF-06946860 ON APPETITE IN PARTICIPANTS WITH ADVANCED CANCER AND ANOREXIA, FOLLOWED BY AN 18-WEEK OPEN-LABEL TREATMENT PERIOD

Pfizer·interventional·Posted Mar 17, 2021·Updated Jan 12, 2024

In Brief

A Phase 1 clinical trial evaluating PF-06946860 and Placebo for PF-06946860 for Non-small Cell Lung Cancer and 9 related conditions. Completed, enrolled 18 participants across 33 sites in 2 countries.

Detailed Summary

Study to compare the effects of the investigational new drug (PF-06946860) and a placebo on appetite and to find out how participants with advanced cancer and anorexia feel after receiving repeated subcutaneous (SC-injected under the skin) doses.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States
Collaborators--

Timeline

Phase 1CompletedFinished
20222023202420252026
First PostedMar 17, 2021
Enrollment StartMay 11, 2021
Primary CompletionApr 14, 2022
Study CompletionAug 9, 2022
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 5.3 years ago

Interventions

PF-06946860drug

subcutaneous injection

Placebo for PF-06946860drug

subcutaneous injection