The trial is taking place at:
S

Summit Cancer Care | Sutlive Street, Savannah, GA

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Buccal Film vs IV Palonosetron for Prevention of CINV in Cancer Patients Receiving MEC

X

Xiamen LP Pharmaceutical

Status and phase

Enrolling
Phase 3

Conditions

Chemotherapy-induced Nausea and Vomiting

Treatments

Drug: IV Palonosetron 0.25 mg
Drug: Palonosetron HCl Buccal Film 0.5 mg

Study type

Interventional

Funder types

Industry

Identifiers

NCT05199818
LP-CT-PALO-202101

Details and patient eligibility

About

The phase 3 study is to compare the efficacy and safety of palonosetron, a long-acting 5-HT3 receptor antagonist, by buccal film delivery compared to IV injection for the prevention of chemotherapy-induced nausea and vomiting. Subjects receive a single dose of palonosetron prior to moderately emetogenic chemotherapy.

Full description

This is a phase 3 randomized, double-blind, parallel group study designed to evaluate the efficacy and safety of palonosetron HCL buccal film versus IV palonosetron for the prevention of chemotherapy-induced nausea and vomiting in cancer patients receiving moderately emetogenic chemotherapy (MEC). Subjects are randomized into two treatment groups, one with the experimental study drug palonosetron in buccal film, the other one with the control treatment using Palonosetron hydrochloride IV injection. Palonosetron PK will be assessed in a subgroup of each treatment group (two sample points, 10% of subjects).

Enrollment

328 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or female, at least 18-years of age;
  • Provide written informed consent;
  • Chemotherapy naïve subject with histologically or cytologically confirmed malignant disease; or chemotherapy non-naïve subject with histologically proven diagnosis of cancer;
  • Karnofsky index ≥ 50;
  • Be scheduled to receive MEC to be administered on Day 1;

Exclusion criteria

  • Unable to understand or cooperate with study procedure;
  • Received any investigational drug 30 days prior to study entry;
  • Used any drug with anti-emetic efficacy 24 hours prior to treatment and during the study;
  • Enrollment in a previous study with palonosetron;
  • Seizure disorder requiring anticonvulsant medication;
  • Experienced any vomiting, retching, or NCI Common Toxicity Criteria grade 2 or 3 nausea in the 24 hours preceding chemotherapy;
  • Ongoing vomiting from any organic etiology;
  • Experienced nausea (moderate to severe or vomiting following any previous chemotherapy);
  • Scheduled to receive moderately or highly-emetogenic chemotherapy or radiotherapy during the study;
  • Known contraindication to 5-HT3 antagonist or dexamethasone;
  • Scheduled to receive bone marrow or stem cell transplant during study;
  • Symptomatic primary or metastatic CNS malignancy;
  • Lactating female.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

328 participants in 2 patient groups

Palonosetron HCl Buccal Film
Experimental group
Description:
Palonosetron HCl Buccal Film 0.5 mg 1 hr before administration of moderately emetogenic chemotherapy and normal saline injection 30 minutes before administration of moderately emetogenic chemotherapy
Treatment:
Drug: Palonosetron HCl Buccal Film 0.5 mg
Palonosetron IV Injection
Active Comparator group
Description:
Placebo buccal film 1 har before administration of moderately emetogenic chemotherapy and Palonosetron HCl Injection 0.25 mg 30 min before administration of moderately emetogenic chemotherapy
Treatment:
Drug: IV Palonosetron 0.25 mg

Trial contacts and locations

13

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Central trial contact

Linhui Cai, MS; Matthew H Nieder, Ph.D.

Data sourced from clinicaltrials.gov

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