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Observational Study on the Use of Akynzeo® in Patients Receiving HEC (EVOLVE_CINV)

Purdue Pharma logo

Purdue Pharma

Status

Completed

Conditions

Chemotherapy-Induced Nausea and Vomiting

Treatments

Drug: 300mg netupitant/0.5mg palonosetron hydrochloride

Study type

Observational

Funder types

Industry

Identifiers

NCT03649230
CAN-PRO-NEPA-001

Details and patient eligibility

About

This Canadian, multi-centre, prospective, observational real-world study is designed to collect patient-reported outcome data on the use of Akynzeo® (netupitant/palonosetron) for the prevention of nausea and vomiting in oncology patients receiving highly emetogenic chemotherapy (HEC).

Full description

The study will assess quality of life using the Functional Living Index of Emesis (FLIE) questionnaire and generate Real World Evidence in support of existing clinical trial data, including effectiveness and safety of Akynzeo® in the real world setting for the prevention of Chemotherapy Induced Nausea and Vomiting (CINV) in patients receiving highly emetogenic chemotherapy (HEC).

Enrollment

207 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects must satisfy the following criteria to be enrolled in the study:

  1. Patient scheduled to receive a highly emetogenic chemotherapy (HEC).
  2. Patient scheduled to receive antiemetic prevention with Akynzeo® according to the approved Canadian Product Monograph as deemed medically necessary by the participating physician independently from this study.
  3. Age ≥ 18 years.
  4. Women of childbearing potential must use effective contraception during therapy and up to one month after treatment with Akynzeo®.
  5. Patient (and/or patient's authorized legal representative) should understand the nature of the study and provide written informed consent prior to or at the screening visit.
  6. Patient is able and willing to comply with the study protocol for the entire length of the study and will follow all study requirements, procedures and complete all visits as required.
  7. Patient is participating in another clinical trial where antiemetic treatment is not pre-specified by the study protocol.

Exclusion criteria

  1. Women of child bearing potential who are pregnant, planning on becoming pregnant or breast feeding.
  2. Hypersensitivity to active substances, excipients or other ingredients of Akynzeo®.
  3. Concomitant use of pimozide, terfenadine, astemizole, or cisapride.
  4. Patient currently enrolled in another clinical trial where antiemetic treatment is pre-specified by the study protocol.

Trial design

Trial documents
1

Trial contacts and locations

17

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Data sourced from clinicaltrials.gov

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