Trial Review

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00973713




Registration number
NCT00973713
Ethics application status
Date submitted
8/09/2009
Date registered
9/09/2009
Date last updated
9/09/2009

Titles & IDs
Public title
Study of RAD001 in Advanced Cholangiocarcinoma: RADiChol
Scientific title
Phase II Study of RAD001 in Advanced Cholangiocarcinoma
Secondary ID [1] 0 0
H2009/3522
Universal Trial Number (UTN)
Trial acronym
RADiChol
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Cholangiocarcinoma 0 0
Condition category
Condition code
Cancer 0 0 0 0
Biliary tree (gall bladder and bile duct)
Oral and Gastrointestinal 0 0 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - RAD001

Experimental: RAD001 10mg/d -


Treatment: Drugs: RAD001
10mg/d
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Tumour control
Timepoint [1] 0 0
12 weeks
Secondary outcome [1] 0 0
Overall survival
Timepoint [1] 0 0
2 years
Secondary outcome [2] 0 0
Toxicity
Timepoint [2] 0 0
2 years

Eligibility
Key inclusion criteria
1. Histologically/cytologically confirmed adenocarcinoma of gall bladder, intra or extra-hepatic biliary tract
2. Metastatic or locally advanced (unresectable) disease
3. Adequate organ function; creatinine<1.5xULN, BR<1.5xULN Neut>1.5, Pts>100
4. WHO Performance status 0-2
5. No prior chemotherapy for advanced Cholangiocarcinoma (Prior adjuvant chemotherapy is accepted)
6. Measurable or non-measurable disease
7. Informed consent for study participation and donation of tumour tissue for evaluation of relevant translational endpoints
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Cytotoxic chemotherapy or immunotherapy within 4 weeks prior to enrolment
2. Prior therapy with mTOR inhibitors (sirolimus, temsirolimus, everolimus)
3. Known intolerance or hypersensitivity to RAD001 (everolimus) or other rapamycins (sirolimus, temsirolimus)
4. Uncontrolled diabetes mellitus or hyperlipidaemia
5. Patients who have any severe and/or uncontrolled medical conditions
6. Active or uncontrolled severe infection
7. Cirrhosis, chronic active hepatitis or chronic persistent hepatitis
8. Severely impaired lung function
9. Patients with a known history of HIV seropositivity
10. Patients who have a history of another primary malignancy (Exceptions include non-melanoma skin cancer, carcinoma in situ of uterine cervix, or any other cancer treated with curative intent without evidence of relapse for more than 2 years)
11. Female patients who are pregnant or nursing (lactating), or adults of reproductive potential who are not using effective birth control methods. If barrier contraceptives are being used, these must be continued throughout the trial by both sexes

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
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
1/09/2009
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/03/2012
Actual
Sample size
Target
27
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Austin Health - Melbourne
Recruitment postcode(s) [1] 0 0
3084 - Melbourne

Funding & Sponsors
Primary sponsor type
Government body
Name
Austin Health
Address
Country

Ethics approval
Ethics application status

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

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Niall Tebbutt, FRACP
Address 0 0
Country 0 0
Phone 0 0
+61394965763
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries

No information has been provided regarding IPD availability


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/NCT00973713