Open Label Trial to Compare BI 207127 to Telaprevir in HCV Patients

Hepatitis C, Chronic Clinical Trial

Official title:

A Phase III, Randomised, Open Label, Active-controlled Study of an Interferon-free Regimen of BI 207127 in Combination With Faldaprevir and Ribavirin Compared to Telaprevir in Combination With Pegylated interferon-a and Ribavirin in Treatment-naive Patients With Chronic Genotype 1b Hepatitis C Virus Infection

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01858961
• Other study ID #: 1241.37
• Secondary ID: 2012-004544-30
• Status: Withdrawn
• Phase: Phase 3
• First received: May 17, 2013
• Last updated: January 22, 2014
• Start date: May 2013
• Est. completion date: July 2016

Study information

• Verified date: January 2014
• Source: Boehringer Ingelheim
• Contact: n/a
• Is FDA regulated: No
• Health authority: Australia: Human Research Ethics CommitteeDenmark: The Danish Health and Medicines AuthorityFrance: Agence Nationale sécurité médicament et des produits santéGermany: Federal Institute for Drugs and Medical DevicesSpain: Spanish Agency of MedicinesSweden: Medical Products Agency
• Study type: Interventional

Clinical Trial Summary

The aim of this trial is to evaluate efficacy and safety of treatment with 600 mg of BID BI 207127 in combination with 120 mg QD Faldaprevir and RBV compared to a Telaprevir-based regimen along with PegIFN and RBV in chronically infected HCV GT1 treatment naïve patients, including patients with compensated cirrhosis.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: July 2016
• Est. primary completion date: July 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion criteria:

1. Chronic HCV, diagnosed by HCV RNA = 1,000 IU/mL at screening in addition to at least one of the following:

1. positive anti-HCV antibodies or detected HCV RNA at least 6 months prior to screening, OR

2. liver biopsy indicating chronic HCV infection, OR

3. history of elevated ALT levels at least 6 months prior to screening.

2. HCV infection of sub-GT1b confirmed by genotypic testing at screening.

3. Treatment naïve defined as:

1. no prior treatment with any interferon, pegylated interferon, and /or ribavirin and

2. no prior treatment with at least one dose of any other licensed or investigational antiviral agent for acute or chronic hepatitis C infection.

4. Availability of a liver biopsy within three years or fibroscan within 6 months prior to randomisation.

Note: patients who do not have a liver biopsy (nor fibroscan) due to contraindication of the procedure should not be excluded for this reason. The decision on the inclusion of these patients should be discussed with the CML. Patients with a liver biopsy performed 3 or more years (or fibroscan performed 6 months or more) prior to randomisation, demonstrating cirrhosis do not need to repeat a liver biopsy or fibroscan.

5. Age 18 - 70 years (inclusive).

6. Female patients

1. with documented hysterectomy, or

2. who have had both ovaries removed, or

3. with documented tubal ligation, or

4. who are post-menopausal with last menstrual period at least 12 months prior to screening, or

5. of childbearing potential with a negative serum pregnancy test at screening and on Day 1 (Visit 2), who agree to use two non-hormonal methods of birth control from the date of screening until 7 months after the last dose of ribavirin. They must not breast-feed at any time from the date of screening until 7 months after the last dose of ribavirin.

Accepted methods of contraception for females in this trial are diaphragm with spermicide substances, intrauterine devices, cervical caps and condoms.

Note: Systemic hormonal contraceptives may not be as effective in women taking BI 207127/FDV combination therapy and are not accepted methods of contraception in the study.

OR:

Male patients

1. who are documented to be sterile, or

2. who consistently and correctly use a condom while their female partners (if of child-bearing potential) agree to use one of the appropriate medically accepted methods of birth control from the date of screening until 7 months after the last dose of ribavirin, and

3. without pregnant female partners. It is in the responsibility of the male patient to ensure that his partner (or partners) is not pregnant prior to enrolment into the study or becomes pregnant during the treatment and follow-up phase. Female partners of childbearing potential must perform monthly pregnancy tests from the date of screening until 7 months after the last dose of ribavirin (tests will be provided by the Sponsor).

7. Signed informed consent form prior to trial participation.

Exclusion criteria:

1. HCV infection of mixed genotype (1/2, 1/3, and 1/4), HCV sub-GT1a or GT1 undefined, diagnosed at screening by genotypic testing.

2. Liver disease due to causes other than chronic HCV infection which may include but is not limited to hemochromatosis, Wilson's disease, or autoimmune liver disease.

3. HIV infection.

4. Hepatitis B virus (HBV) infection based on presence of Hepatitis B surface antigen.

5. Evidence of decompensated liver disease or history of decompensated liver disease, defined as history of ascites, hepatic encephalopathy, bleeding esophageal varices or any other evidence of previous decompensation and/or any laboratory results (International Normalised Ratio, albumin, bilirubin) indicating a Child-Pugh-Turcotte score > 6 points (i.e. CPT-B or -C)

6. Confirmed or suspected active malignancy or history of malignancy within the last 5 years (with the exception of appropriately treated basal cell carcinoma of the skin or in situ carcinoma of the uterine cervix).

7. Patients with ongoing or historical photosensitivity or recurrent rash.

8. History of illicit drug use (other than cannabis) or chronic alcohol abuse within 12 months prior to randomization, in the opinion of the Investigator.

9. Body mass index <18 or >35 kg/m2.

10. Usage of any investigational drugs within 28 days prior to randomisation, or the planned usage of an investigational drug during the course of the current study.

11. Known hypersensitivity to any ingredient of the study drugs.

12. A condition that is insufficiently diagnosed, treated or clinically unstable which in the opinion of Investigator may put the patient at risk because of participation in this study, influence the results of this study, or limit the patient's ability to participate in this study.

13. Alpha fetoprotein value >100ng/mL at screening; if > 20ng/mL and = 100ng/mL, patients can be included if there is no evidence of liver cancer in an appropriate imaging study within 6 months prior to randomisation.

14. A history of severe pre-existing cardiac disease, including unstable or uncontrolled cardiac disease (e.g. congestive heart failure, myocardial infarction, unstable angina and arrhythmic disorders) current or within the previous 12 months before randomisation. Clinically significant Electrocardiogram (ECG) abnormalities. A history of congenital QT prolongation, or a family history of congenital QT prolongation or sudden death.

15. Received silymarin (milk thistle) or glycyrrhizin or Sho-saiko-to (SST) within 28 days prior to randomisation or any medication listed in a restricted medication list provided in ISF within 28 days prior to randomisation, with the exception of parenteral analgesics used during liver biopsy procedure.

16. Pre-existing psychiatric conditions that could interfere with the subject's participation in and completion of the study including but not limited to severe depression or hospitalization for depression, suicidal ideation and attempted suicide, schizophrenia, bipolar illness, severe anxiety or personality disorder, history of craniocerebral trauma or active seizure disorders requiring medication, a period of disability or impairment due to a psychiatric disease current or within the previous 3 years before randomisation.

17. Abnormal thyroid function that cannot be controlled effectively by medication.

18. Active autoimmune-mediated disease (e.g., Crohn's disease, ulcerative colitis, idiopathic thrombocytopenic purpura, systemic lupus erythematosus, autoimmune hemolytic anemia, scleroderma, severe psoriasis).

19. Requirement for chronic systemic corticosteroids (inhaled or nasally administered or pulmonary steroids will be allowed).

20. History or other evidence of severe retinopathy or clinically significant ophthalmological disorder due to diabetes mellitus or hypertension (but not limited to these conditions).

Plus other exclusion criteria relating to Peg interferon, ribavirin and Telaprevir.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Hepatitis
• Hepatitis C
• Hepatitis C, Chronic

Intervention

Drug:
• BI 201335
Once a day
• ribavirin
Twice a day
• BI 207127
Twice a day
• Telaprevir
Three times a day
• ribavirin
Twice a day
• Pegylated Interferon
Once a week

Locations

Country	Name	City	State
Australia	1241.37.61001 Boehringer Ingelheim Investigational Site	Adelaide	South Australia
Australia	1241.37.61003 Boehringer Ingelheim Investigational Site	Fitzroy	Victoria
Australia	1241.37.61002 Boehringer Ingelheim Investigational Site	Westmead	New South Wales
Spain	1241.37.34010 Boehringer Ingelheim Investigational Site	Alzira
Spain	1241.37.34005 Boehringer Ingelheim Investigational Site	Barcelona
Spain	1241.37.34002 Boehringer Ingelheim Investigational Site	L'Hospitalet Llobregat (BCN)
Spain	1241.37.34001 Boehringer Ingelheim Investigational Site	Madrid
Spain	1241.37.34003 Boehringer Ingelheim Investigational Site	Madrid
Spain	1241.37.34004 Boehringer Ingelheim Investigational Site	Madrid
Spain	1241.37.34006 Boehringer Ingelheim Investigational Site	Valencia
Sweden	1241.37.46002 Boehringer Ingelheim Investigational Site	Lund
Sweden	1241.37.46001 Boehringer Ingelheim Investigational Site	Stockholm

Sponsors (1)

Lead Sponsor	Collaborator
Boehringer Ingelheim

Countries where clinical trial is conducted

Australia,  Spain,  Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Sustained Virologic Response at Week 12 after end of treatment (SVR12)		at week 12 post treatment	No
Secondary	SVR4: Plasma HCV RNA level <25 IU/mL1 at 4 weeks after end of treatment		at week 4 post treatment	No
Secondary	SVR24: Plasma HCV RNA level <25 IU/mL1 at 24 weeks after end of treatment		at week 4 post treatment	No
Secondary	Virological Response at Week 4 -Plasma HCV RNA level undetectable at Week 4 -Plasma HCV RNA level <25 IU/mL at Week 4		at week 4 post treatment	No
Secondary	Plasma HCV level undetectable at Week 12		at week 12	No
Secondary	Time to achieving HCV RNA undetectable		up to week 48	No
Secondary	Virological breakthrough		up to week 48	No
Secondary	ETR: Plasma HCV RNA level undetected at the end of treatment		week 24 or 48	No
Secondary	Lack of on-treatment viral response		up to week 48	No
Secondary	Relapse		up to 48 weeks post treatment	No
Secondary	Adverse events		up to week 48 post treatment	Yes
Secondary	Adverse events leading to discontinuation		up to week 48	Yes
Secondary	Serious Adverse Events		up to week 48 post treatment	Yes
Secondary	Laboratory test abnormalities by DAIDS grades		up to week 48 post treatment	Yes
Secondary	Rate of red blood cell transfusion		up to week 48 post treatment	Yes
Secondary	Time to discontinuation of trial medication		up to week 48	No
Secondary	Liver disease progression, fibroscan and FibroSURE		up to week 48 post treatment	No
Secondary	Rate of ESA use		up to week 48 post treatment	Yes
Secondary	Change in laboratory test values over time		up to week 48 post treatment	Yes
Secondary	Patients requiring hospitalisation due to AEs related to study drugs		up to week 48 post treatment	Yes