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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT00801255




Registration number
NCT00801255
Ethics application status
Date submitted
2/12/2008
Date registered
3/12/2008
Date last updated
2/11/2016

Titles & IDs
Public title
A Study of Combination Treatment With an HCV Polymerase Inhibitor (RO5024048) and an HCV Protease Inhibitor (RO5190591/Danoprevir) in Genotype 1 Chronic Hepatitis C Patients
Scientific title
A Randomized, Placebo-controlled, Dose-ranging Study to Evaluate the Safety, Tolerability and Antiviral Activity of Combination Treatment With an HCV Polymerase Inhibitor (RO5024048) and an HCV Protease Inhibitor (RO5190591) in Genotype 1 Chronic Hepatitis C Patients. INFORM 1
Secondary ID [1] 0 0
PP22205
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Hepatitis C, Chronic 0 0
Condition category
Condition code
Infection 0 0 0 0
Other infectious diseases
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 - RO5024048
Treatment: Drugs - danoprevir
Treatment: Drugs - danoprevir
Treatment: Drugs - danoprevir
Treatment: Drugs - danoprevir
Treatment: Drugs - danoprevir

Experimental: Cohort A -

Experimental: Cohort B -

Experimental: Cohort C -

Experimental: Cohort D -

Experimental: Cohort E -

Experimental: Cohort F -

Experimental: Cohort G -


Treatment: Drugs: RO5024048
500mg po bid/100mg po q8h for 7 days

Treatment: Drugs: danoprevir
500mg po bid/100mg po q8h for 14 days

Treatment: Drugs: danoprevir
1000mg po bid/100mg po q8h for 14 days\n500mg po bid/200mg po q8h for 14 days

Treatment: Drugs: danoprevir
1000mg po bid/200mg po q8h for 14 days

Treatment: Drugs: danoprevir
1000mg/600mg po twice daily for 14 days

Treatment: Drugs: danoprevir
1000mg/900mg po twice daily for 14 days
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
HCV RNA
Timepoint [1] 0 0
At each clinic visit, throughout study
Primary outcome [2] 0 0
Adverse events, laboratory parameters, vital signs
Timepoint [2] 0 0
At each clinic visit, throughout study
Secondary outcome [1] 0 0
PK parameters;viral resistance
Timepoint [1] 0 0
At intervals, throughout study

Eligibility
Key inclusion criteria
- adult patients, 18-65 years of age;

- chronic hepatitis C, genotype 1.
Minimum age
18 Years
Maximum age
65 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- decompensated liver disease, or impaired liver function;

- presence or history of non-hepatitis C chronic liver disease;

- HBsAg or HIV infection;

- history of cancer within 5 years, other than localized or in situ cancer of the skin.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled 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
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/11/2008
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/03/2010
Sample size
Target
Accrual to date
Final
88
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
- Adelaide
Recruitment hospital [2] 0 0
- Heidelberg
Recruitment hospital [3] 0 0
- Melbourne
Recruitment postcode(s) [1] 0 0
SA 5000 - Adelaide
Recruitment postcode(s) [2] 0 0
3084 - Heidelberg
Recruitment postcode(s) [3] 0 0
3181 - Melbourne
Recruitment outside Australia
Country [1] 0 0
New Zealand
State/province [1] 0 0
Christchurch
Country [2] 0 0
New Zealand
State/province [2] 0 0
Grafton

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Hoffmann-La Roche
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
This 7 cohort study will evaluate the efficacy and safety of combination treatment with an
HCV nucleoside polymerase inhibitor(RO5024048)and an HCV protease
inhibitor(RO5190591/ITMN-191/danoprevir) in patients with chronic hepatitis C, genotype
1.Cohorts A,B,C,D and G will be treatment-naive patients, cohort E will be
treatment-experienced excluding null responders, and cohort F will be null responders.
Cohorts A and B will evaluate doses of 500mg po bid RO5024048 and 100mg po q8h RO5190591,
alone or in combination, for up to 7 or 14 days. Cohort C will evaluate combination treatment
with either 1000mg po bid RO5024048 and 100mg q8h RO5190591 or 500mg po bid RO5024048 and
200mg q8h RO5190591 for 14 days. Cohort D will evaluate 1000mg po bid RO5024048 and 200mg q8h
RO5190591 for 14 days.Cohort E will evaluate 1000mg RO5024048/600mg RO5190591 po twice daily
for 14 days, and Cohorts F and G will evaluate 1000mg RO5024048/900mg RO5190591 po twice
daily for 14 days. Cohorts will be tested sequentially or in parallel, if supported by
appropriate safety and pharmacokinetic data.Following the last dose of study medication
patients have the option of continuing treatment with Standard of care therapies. The
anticipated time on study treatment is <3 months, and the target sample size is <100
individuals.
Trial website
https://clinicaltrials.gov/ct2/show/NCT00801255
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Clinical Trials
Address 0 0
Hoffmann-La Roche
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
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 are available at https://clinicaltrials.gov/ct2/show/NCT00801255