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NCT04252612

Biological Outcomes of Pramlintide in Resectable Cutaneous Squamous Cell Carcinoma: A Pilot Study

Withdrawn EARLY_PHASE1 Last updated 28 June 2023
What this trial tests

EARLY_PHASE1 trial testing Pramlintide in Cutaneous Squamous Cell Carcinoma. Withdrawn.

Timeline
30 January 2020
Primary endpoint
26 June 2023
26 June 2023

Quick facts

Lead sponsorH. Lee Moffitt Cancer Center and Research Institute
PhaseEARLY_PHASE1
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Start date30 January 2020
Primary completion26 June 2023
Estimated completion26 June 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

H. Lee Moffitt Cancer Center and Research Institute

Who can join

18 and older, any sex, with Cutaneous Squamous Cell Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will treat resectable cutaneous squamous cell carcinoma patients with pramlintide for two weeks prior to surgical resection of their tumor. Pre-treatment and surgical resection specimens will then be analyzed for biological alterations.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Pramlintide

Trials testing the same drug.

Other recruiting trials for Cutaneous Squamous Cell Carcinoma

Currently open trials in the same condition.

Other H. Lee Moffitt Cancer Center and Research Institute trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04252612.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing