Overview

This trial is active, not recruiting.

Condition hepatitis b, chronic
Treatments rep 2139-ca, pegylated interferon, entecavir
Phase phase 2
Sponsor Replicor Inc.
Start date October 2012
End date September 2016
Trial size 5 participants
Trial identifier NCT02726789, REP 201

Summary

The REP 201 protocol is a small exploratory study assessing the antiviral effects and tolerability of REP 2139-Ca when used with a full course of pegylated interferon (48 weeks) in treatment naive patients or in patients already receiving entecavir and continuing entecavir with treatment.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
treatment naive patients receive REP 2139-Ca in combination with pegylated interferon.
rep 2139-ca
the nucleic acid polymer REP 2139 formulated as a calcium chelate complex
pegylated interferon pegylated interferon alpha 2a, Pegasys(R)
immunotherapy
(Experimental)
patients with previous entecavir exposure receive REP 2139-Ca in combination with pegylated interferon while continuing their entecavir therapy.
rep 2139-ca
the nucleic acid polymer REP 2139 formulated as a calcium chelate complex
pegylated interferon pegylated interferon alpha 2a, Pegasys(R)
immunotherapy
entecavir local generic entecavir
local generic entecavir

Primary Outcomes

Measure
Number of patients experiencing treatment emergent laboratory test abnormalities or adverse events.
time frame: 48 weeks (treatment)

Secondary Outcomes

Measure
Number of patients experiencing reductions in serum HBsAg
time frame: 48 weeks (treatment)
Number of patients experiencing reductions in serum HBeAg
time frame: 48 weeks (treatment)
Number of patients experiencing reductions in serum HBV DNA
time frame: 48 weeks (treatment)
Number of patients experiencing serum anti-HBs > 10 mIU / ml
time frame: 48 weeks (treatment)
Number of patients experiencing HBeAg seroconversion
time frame: 48 weeks (treatment)

Eligibility Criteria

Male or female participants from 18 years up to 55 years old.

Inclusion Criteria: - Age between 18 and 55 - HBsAg+ - Anti-HBs negative - Patients currently receiving nucleoside based HBV polymerase inhibitors may be included in the study at the discretion of the Principle Investigator. - HIV / hepatitis C / hepatitis delta virus negative - Fibrosis with compensation (as determined by Fibroscan and liver enzymes) - Non cirrhotic - No known active cytomegalovirus infection - Willingness to utilize adequate contraception while being treated with REP 9AC' and for 6 months following the end of treatment - Adequate venous access allowing weekly intravenous therapies and blood tests Exclusion Criteria: - Evidence of cardiovascular disease - Autoimmune hepatitis - Presence of Wilson's disease - Presence of severe NAFLD - Evidence of any other co-existent liver disease - Anti-nuclear antibody positive - Ultrasonograph of hepato-biliary system: positive for cirrhosis of liver - A history of ascites, hepatic encephalopathy or variceal hemorrhage - Body weight > 100 kg - Platelet count < 75,000, polymorphonuclear cell count < 1,500 or hematocrit < 33% - alpha feto protein > 100 ng/ml or the presence of a hepatic mass suggestive of hepatocellular carcinoma . - Bilirubin > 2.5 mg/dl - Creatinine > 1.5 mg/dl - Platelet count < 75,000 / cmm - Serum albumin < 35 mg/ml - Poorly controlled diabetes mellitus - Another serious medical disorder - A serious psychiatric disorder - Uncontrolled hypertension - A history of alcohol abuse within the last year - The use of illicit drugs within the past two years - Inability to provide informed consent - Positive pregnancy test - Breastfeeding - Inability or unwillingness to provide weekly blood samples - Poor venous access making IV infusion too difficult

Additional Information

Official title Therapeutic Safety and Efficacy of Combination Treatment With REP 2139-Ca and Pegasys in Patients With Chronic Hepatitis B
Principal investigator Mamun Al-Mahtab, MD
Description Chronic hepatitis B is a long term condition caused by infection of the body with the hepatitis B virus (HBV). This infection often results in inflammation or scarring of the liver and can eventually lead to liver cirrhosis and liver failure. These infections are also one of the major causes of the development of hepatocellular carcinoma (liver cancer). Although some drugs have been approved to treat chronic hepatitis B infections, they do not provide a complete cure except in rare cases (a cure generally means that a person loses the hepatitis B virus from the blood and the liver and develops a durable immunological control of subsequent HBV infection). However, these drugs do significantly decrease the risk of liver damage and liver cancer arising from the presence of a chronic liver infection by slowing or stopping the production of infectious virus. Thus the primary problem associated with currently available drugs is the lack of clearance of the virus from the hepatocytes which necessitates long term treatment with these drugs. There is clearly a need to identify new drugs that can benefit patients with chronic hepatitis B infections. Nucleic acid-based polymers (NAPs) are a new class of broad-spectrum antiviral compounds which act against HBV infection by blocking the release of the surface antigen protein (HBsAg) from infected hepatocytes. Current interim data analysis from the REP 102 assessing the activity of the NAP REP 9AC' (REP 2139, given as a calcium chelate complex [REP 2139-Ca]) in patients with chronic HBV infection indicates the following: 1. REP 2139-Ca is generally well tolerated and patients tolerate short term combined treatment (13-26 weeks) of pegylated interferon and / or thymosin alpha 2. REP 2139-Ca has achieved serum HBsAg reduction or clearance 9 of 9 patients receiving combined therapy. 3. Appearance of substantial titers of serum anti-HBs occur with the addition of immunotherapy. 4. After all treatment is withdrawn, 8 / 9 patients achieved HBV DNA < 116 copies / ml (LLOQ of the Roche Cobas platform) and sustained suppression of viremia (HBV DNA < 1000 cpm, HBsAg < 1 IU / ml) for a period of greater than 1 year was observed in four patients. This exploratory study is designed to examine if REP 2139-Ca can be safely combined with a full course of pegylated interferon in treatment naive patients and in patients with previous and continuing therapy with entecavir and that similar antiviral effects can be observed as in the previous REP 101 and 102 protocols.
Trial information was received from ClinicalTrials.gov and was last updated in March 2016.
Information provided to ClinicalTrials.gov by Replicor Inc..