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NCT04826432: PASIREOCHIP

Pasireotide to Reduce Clinically Relevant Digestive Leakage After Complete Cytoreductive Surgery (CRS) Plus Hyperthermic Intra-Peritoneal Chemotherapy (HIPEC) for Peritoneal Carcinomatosis

Terminated Phase 2 Last updated 8 February 2024
What this trial tests

Phase 2 trial testing Pasireotide 0.9 MG/ML in Peritoneal Carcinomatosis in 6 participants. Terminated before completion.

Timeline
3 September 2020
Primary endpoint
7 February 2024
7 February 2024

Quick facts

Lead sponsorGustave Roussy, Cancer Campus, Grand Paris
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment6
Start date3 September 2020
Primary completion7 February 2024
Estimated completion7 February 2024
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Gustave Roussy, Cancer Campus, Grand Paris — full company profile →

Who can join

Adults 18 to 75, any sex, with Peritoneal Carcinomatosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To assess the efficacy of pasireotide in the reduction of clinically relevant postoperative digestive leakage after CRS plus HIPEC compared to placebo

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Pasireotide 0.9 MG/ML

Trials testing the same drug.

Other recruiting trials for Peritoneal Carcinomatosis

Currently open trials in the same condition.

Other Gustave Roussy, Cancer Campus, Grand Paris 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/NCT04826432.

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