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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT03188159




Registration number
NCT03188159
Ethics application status
Date submitted
16/03/2017
Date registered
15/06/2017

Titles & IDs
Public title
Vinorelbine in Relapsed Platinum Resistant or Refractory C5 High Grade Serous, Endometrioid, or Undifferentiated Primary Peritoneum, Fallopian Tube or Ovarian Cancer
Scientific title
Phase II Study of Intravenous Vinorelbine in Patients With Relapsed Platinum Resistant or Refractory C5 High Grade Serous, Endometrioid, or Undifferentiated Primary Peritoneum, Fallopian Tube or Ovarian Cancer (VIP)
Secondary ID [1] 0 0
GY01/05/16
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Ovarian Cancer 0 0
Fallopian Tube Cancer 0 0
Condition category
Condition code
Cancer 0 0 0 0
Ovarian and primary peritoneal
Cancer 0 0 0 0
Womb (Uterine or endometrial cancer)

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Vinorelbine

Experimental: IV Vinorelbine - IV Vinorelbine 25mg/m2


Treatment: Drugs: Vinorelbine
Vinorelbine 25 mg/m2 intravenously on day-1 and day-8 of a 3 week cycle to commence following confirmation of eligibility into the study for a maximum of 12 months, until disease progression, intolerable toxicity or withdrawal of patient consent (whichever event occurs first).
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Response rates
Timepoint [1] 0 0
3 years
Secondary outcome [1] 0 0
Progression free survival
Timepoint [1] 0 0
3 years
Secondary outcome [2] 0 0
Changes in the level of CA 125
Timepoint [2] 0 0
3 years
Secondary outcome [3] 0 0
Adverse event profile
Timepoint [3] 0 0
3 years

Eligibility
Key inclusion criteria
1. Provided written informed consent
2. Patients must have platinum resistant or refractory HGSOC; defined as progressive disease by imaging = 6 months from last date of most recent platinum-based therapy or rising CA-125 based on GCIG criteria
3. Have histological confirmation of high-grade serous or high-grade endometrioid or undifferentiated tumour of the primary peritoneum, fallopian tube cancer or ovary
4. Molecular subtyping by Nanostring technology must confirm C5 subtype on primary ovarian surgical sample or a biopsy of recurrent disease
5. Patients must not have received more than 3 prior chemotherapy regimens, which may include chemotherapy, biologics or other targeted therapies (this does not include maintenance treatment or hormonal therapy) for platinum resistant disease
6. Measurable disease by RECIST criteria (version 1.1).
7. At time of registration, if the patient has had previous treatment it must have been at least 28 days since major surgery or radiation therapy; 28 days from any other previous anti-cancer therapy including biologics; 14 days since hormone therapy. Patients must have recovered to = grade 1 from their treatment-related events with the exception of alopecia.
8. Age = 18 years of age (Age = 21 years of age for Singapore sites)
9. Have clinically acceptable laboratory screening results within certain limits specified below:

* AST and ALT = 2.5 times upper limit of normal (ULN)
* Total bilirubin = ULN
* Creatinine = 1.5 x UL
* Absolute neutrophil count = 1500 cells/mm
* Platelets = 100,000/mm3
* Hemoglobin = 9.0 g/dl
10. Have an ECOG performance status of = 2.
11. Women of child-producing potential must agree to use effective contraceptive methods prior to study entry, during study participation, and for at least 30 days after the last administration of study medication.
12. Have the ability to understand the requirements of the study, provide written informed consent, abide by the study restrictions, and agree to return for the required assessments.
13. Able to tolerate IV medication.
14. Life expectancy greater than 6 months
Minimum age
21 Years
Maximum age
99 Years
Sex
Females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Women who are pregnant or nursing
2. Previous exposure to vinorelbine
3. Patients known to be hypersensitive to vinorelbine or any vinca alkaloids previously
4. Persistent toxicities (= Common Terminology Criteria for Adverse Event (CTCAE) v4.0 grade 1) caused by previous cancer therapy, excluding alopecia
5. Have active, acute, or chronic clinically significant infections or bleeding.
6. Have active angina pectoris, stroke, myocardial infarction, or any other pre-existing uncontrolled cardiovascular condition within the last 6 months.
7. Have additional uncontrolled serious medical or psychiatric illness.
8. Require therapeutic doses of anti-coagulation with warfarin or warfarin derivatives. However, treatment with low molecular weight heparin (LMWH) is allowed.
9. Known symptomatic CNS metastases. Treated brain metastatis that are stable for more than =4 weeks are allowed.
10. Psychiatric disorders that would hinder compliance with study protocol
11. History of other malignancies within the past 5 years except for curatively treated skin BCC or SCC or cervical carcinoma in situ. Patients who have had curatively treated breast cancer, with completion of adjuvant chemotherapy more than three years before are allowed.
12. Require treatment with drugs known to be potent inducers or inhibitors of CYP3A4 at the time of registration
13. Subjects known to be HIV positive or with active and untreated Hepatitis B or Hepatitis C infection. Patients with controlled Hepatitis B or Hepatitis C infection on treatment with antiviral medication are allowed.

Study design
Purpose of the study
Treatment
Allocation to intervention
NA
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 2
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
UNKNOWN
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/07/2017
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/07/2022
Actual
Sample size
Target
36
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
Peter MacCallum Cancer Centre - Melbourne
Recruitment postcode(s) [1] 0 0
- Melbourne
Recruitment outside Australia
Country [1] 0 0
Singapore
State/province [1] 0 0
Singapore

Funding & Sponsors
Primary sponsor type
Other
Name
National University Hospital, Singapore
Address
Country
Other collaborator category [1] 0 0
Other
Name [1] 0 0
National Cancer Centre, Singapore
Address [1] 0 0
Country [1] 0 0
Other collaborator category [2] 0 0
Government body
Name [2] 0 0
KK Women's and Children's Hospital
Address [2] 0 0
Country [2] 0 0
Other collaborator category [3] 0 0
Other
Name [3] 0 0
Australia New Zealand Gynaecological Oncology Group
Address [3] 0 0
Country [3] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
David Tan
Address 0 0
National University Hospital, Singapore
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
David SP Tan
Address 0 0
Country 0 0
Phone 0 0
(65) 6779 5555
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT03188159