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Clinical Trials/EUCTR2018-004844-43-HU
EUCTR2018-004844-43-HU
Active, not recruiting
Phase 1

A Phase 4, Open-label, Single Arm Study to Evaluate the Safety and Tolerability of a Three-day Fosaprepitant Regimen Administered for the Prevention of Chemotherapy-Induced Nausea and Vomiting (CINV) in Pediatric Participants Receiving Emetogenic Chemotherapy

Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.0 sites100 target enrollmentJuly 8, 2019
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DrugsIVEMEND®

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
Enrollment
100
Status
Active, not recruiting
Last Updated
5 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 8, 2019
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •To be eligible for inclusion in this study, the participant must:
  • •1\. Be receiving a moderately or highly emetogenic chemotherapy agent/regimen or a chemotherapy agent/regimen not previously tolerated due to vomiting.
  • •2\. Have a Lansky Play Performance score \=60 (participants \=16 years of age) or a Karnofsky score \=60 (participants \>16 years of age).
  • •3\. Have a preexisting functional central venous catheter available for study intervention administration.
  • •4\. Be fosaprepitant naïve.
  • •5\. Have a predicted life expectancy \=3 months.
  • •6\. Be male or female.
  • •A female participant is eligible to participate if she is not pregnant or breastfeeding, and at least one of the following conditions applies:
  • •\- Is not a woman of childbearing potential (WOCBP) OR
  • •\- Is a WOCBP and agrees to the following for at least 28 days prior to receiving study intervention, during the intervention period, and for at least 30 days (or local standard of care if longer) after the last dose of study intervention (including the optional cycles):

Exclusion Criteria

  • •The participant must be excluded from the study if the participant:
  • •1\. Has abnormal laboratory values as follows:
  • •\- peripheral absolute neutrophil count (ANC) \<1000/mm3
  • •\- platelet count \<75,000/mm3
  • •\- aspartate aminotransferase (AST) \>5\.0 × upper limit of normal (ULN) for age
  • •\- alanine aminotransferase (ALT) \>5\.0 × ULN for age
  • •\- bilirubin \>1\.5 × ULN for age
  • •\- creatinine \>1\.5 × ULN for age
  • •2\. Will receive stem cell rescue therapy in conjunction with a study\-related course of emetogenic chemotherapy or during the 14 days following administration of fosaprepitant.
  • •3\. Is currently a user of any recreational or illicit drugs or has current evidence of drug or alcohol abuse or dependence as determined by the investigator.

Outcomes

Primary Outcomes

Not specified

Similar Trials

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Phase 4
A Phase 4, Open-label, Single Arm Study to Evaluate the Safety and Tolerability of a Three-day Fosaprepitant Regimen Administered for the Prevention of Chemotherapy-Induced Nausea and Vomiting (CINV) in Pediatric Participants Receiving Emetogenic ChemotherapySymptomen en algemene pathologieChemotherapy-Induced Nausea and Vomiting
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Three-day Fosaprepitant Regimen CINV Safety Study in Pediatric ParticipantsPrevention of Chemotherapy-Induced Nausea and Vomiting (CINV)MedDRA version: 20.1Level: PTClassification code 10054133Term: Prophylaxis of nausea and vomitingSystem Organ Class: 10042613 - Surgical and medical proceduresTherapeutic area: Diseases [C] - Symptoms and general pathology [C23]
EUCTR2018-004844-43-LTMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.100