Granisetron Extended Release Injection (GERSC) for the Prevention of Chemotherapy-induced Nausea and Vomiting

The University of Alabama at Birmingham

Status and phase

Withdrawn

Phase 2

Conditions

Chemotherapy-induced Nausea and Vomiting

Treatments

Drug: GRANISETRON EXTENDED RELEASE INJECTION (GERSC)

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT04085393

UAB1950

Details and patient eligibility

About

Chemotherapy-induced nausea and vomiting (CINV) adversely affects patients' quality of life and may affect patients' treatment decisions. The emetogenicity of the chemotherapy administered and specific patient characteristics such as female gender, age, and history of low alcohol intake can increase a patients' risk for CINV.

GERSC is a new, subcutaneously (SC) administered polymeric formulation of Granisetron that was developed to provide slow, controlled, and sustained release of Granisetron to prevent both acute and delayed CINV associated with moderately emetic chemotherapy (MEC) and highly emetic chemotherapy (HEC)

Full description

All patients eligible for the study receiving moderately emetogenic (MEC) chemotherapy will receive GERSC receptor antagonist on day one. All patients eligible for the study receiving highly emetogenic Chemotherapy (HEC) chemotherapy will receive GERSC receptor antagonist on day one including dexamethasone and NK-1 Receptor antagonist during cycle 1.

The primary objective is to measure the Complete Response (no emetic episodes, no use of rescue medications) in patients receiving GERSC as a replacement for the second generation 5 HT3 receptor antagonist palonosetron used in the first chemotherapy cycle for those patients receiving MEC or HEC and developed Breakthrough CINV. Complete response would be recorded specifically for the acute (0-24 hours post-chemotherapy), delayed (24-120 hours post-chemotherapy), and overall periods (0-120 hours post-chemotherapy).

This study has two study groups.

Group 1 (HEC) will receive GERSC, dexamethasone and NK-1 antagonist prior to chemotherapy
Group 2 (MEC) will receive GERSC and dexamethasone prior to chemotherapy

During the study:

Participants will be completing questionnaires on day 1 prior to treatment and at approximately the same time treatment was given each day for the next seven days. Participant will be assessed each day on the amount of nausea, vomiting, and/or sedation experienced in the previous 24-hour period. The assessment should take less than 5 minutes to complete each day.

Participants will be registered for Quality of Life measurement. Validated QOL measurements of fatigue and overall perception of QOL will be assessed upon registration in this study. Fatigue and overall well-being clearly can impact how well patients will do in terms of being able to tolerate and experience nausea and vomiting

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Diagnosis of malignant disease and scheduled for MEC or HEC
Chemotherapy naive
Age ≥18 years.
ECOG Performance Status 0 or 1
Required Initial Laboratory Values ≤28 days prior to registration. Patient must have adequate bone marrow, kidney, and liver function as evidenced by:
Platelet count ≥ 100,000/ mm3
Bilirubin ≤ 1.5 x ULN, except for subjects with Gilbert's syndrome
Serum Creatinine ≤2.0 mg/dL
SGOT or SGPT ≤3 x upper limit of normal (ULN)
Absolute neutrophil count (ANC) ≥1500/mm3
Patients receiving HEC will have received the 5HT3 receptor antagonist palonosetron, a NK-1, and dexamethasone as antiemetic prophylaxis during cycle 1 of chemotherapy
Patients receiving MEC will have received the 5HT3 receptor antagonist palonosetron, and dexamethasone as antiemetic prophylaxis during cycle 1 of chemotherapy

Exclusion criteria

No nausea or vomiting ≤ 24 hours prior to registration.
Negative pregnancy test (serum β hCG) done ≤7 days prior to registration, for women of childbearing potential only (per clinician discretion).
No severe cognitive compromise.
No known history of active, untreated CNS disease (e.g. brain metastases, seizure disorder).
No concurrent use of amifostine, thioridazine, pimozide or St. John's wort.
No concurrent abdominal radiotherapy.
No concurrent use of olanzapine therapy.
No chronic alcoholism (as determined by the investigator).
No known hypersensitivity to granisetron.
No known uncontrolled cardiac arrhythmia or uncontrolled congestive heart failure.
No acute myocardial infarction within the previous six months.
No history of uncontrolled diabetes mellitus (may be on a stable dose of insulin or on a stable dose of an oral hypoglycemic agent).
Patients with psychiatric illness that would prevent the patient from giving informed consent are not eligible for the trial
Medical condition such as uncontrolled infection (including HIV),uncontrolled Diabetes Mellitus, unstable cardiac disease which, in the opinion of the treating physician, would make this protocol unreasonably hazardous for the patient are not eligible for the trial
Patients with a "currently active" second malignancy other than non-melanoma skin cancers are not eligible for the trial; Patients are not considered to have a "currently active" malignancy if they have completed therapy and are free of disease for ≥ 3 years.
Patients who cannot swallow oral formulations of the agent(s) are not eligible for the trial.