A Phase I/II Clinical Trial With Interferon Alfa 5 in Treatment-Experienced Patients With Genotype-1 Chronic Hepatitis C
This study has been completed.
Sponsor:
Digna Biotech S.L.
Information provided by (Responsible Party):
Digna Biotech S.L.
ClinicalTrials.gov Identifier:
NCT01121731
First received: May 10, 2010
Last updated: February 4, 2013
Last verified: February 2013
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Purpose
The general aim of this study is to determine if 3 MIU of IFN-α5 in monotherapy, and 1,5 MIU of IFN-α5 combined with 1,5 MIU of IFN- α2b, are safe dose levels as well as to investigate the antiviral efficacy and pharmacodynamics (PD) of such doses and drugs in treatment-experienced HCV patients with genotype 1 chronic infection, after 29 days of treatment. It is also intended to determine pharmacokinetics (PK) of the safe dose achieved of IFN-α5 in monotherapy.
| Condition | Intervention | Phase |
|---|---|---|
|
Chronic Hepatitis C Virus Infection Genotype 1 Treatment-Experienced Patients Relapses |
Drug: Interferon α-5 Drug: Interferon-α5 plus Interferon-α 2b Drug: Interferon α-2b (INTRON® A) |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Phase I/II, Multicenter, Randomized, Open,Active-Controlled, ClinicalTrial to Evaluate PK, PD, Safety and Tolerability Of Interferon Alfa 5, S.C. 3 Times Per Week, For 29 Days, To Treat-Experienced Pat. With Genotype-1 Chronic Hepatitis C |
Resource links provided by NLM:
Drug Information available for:
Interferon
Interferon Alfa-2a
Interferon Alfa-2b
Hepatitis A Vaccines
U.S. FDA Resources
Further study details as provided by Digna Biotech S.L.:
Primary Outcome Measures:
- Safe dose level [ Time Frame: 29 days of treatment ] [ Designated as safety issue: Yes ]
PRIMARY ENDPOINTS OF PHASE I
- To determine if 3 MIU of IFN-α5 are well tolerated and if not, to find a safe dose level for IFN-α5.
- To determine if 1.5 MIU of IFN-α5 in combination with 1.5 MIU of IFN-α2b (IFN-α5 + IFN-α2b) are well tolerated and if not, to find a safe dose level for the combination of IFN-α5 and IFN-α2b.
PRIMARY ENDPOINTS OF PHASE II
- To analyze IFN-α5 preliminary antiviral efficacy at the dose of 3 MIU, or the safe dose level identified in Phase I.
- Primary safety endpoints: Occurrence of AE (classified into mild, moderate and severe)
Secondary Outcome Measures:
- pharmacodynamic and pharmacokinetic parameters [ Time Frame: 29 days of treatment ] [ Designated as safety issue: No ]
SECONDARY ENDPOINTS OF PHASE I
- To obtain pharmacokinetic parameters of IFN-α5 in monotherapy after single and multiple dose administration
- To obtain pharmacodynamic parameters of IFN-α5 in monotherapy and in combination with IFN-α2b
SECONDARY ENDPOINTS OF PHASE II
- To analyze IFN-α5 + IFN-α2b preliminary antiviral efficacy and comparison between IFN-α5 in monotherapy, IFN-α5 + IFN-α2b and IFN-α2b in monotherapy.
- To obtain pharmacodynamic parameters after treatment with IFN-α5, IFN-α5 + IFN-α2b or IFN-α2b.
| Enrollment: | 70 |
| Study Start Date: | May 2010 |
| Study Completion Date: | January 2013 |
| Primary Completion Date: | October 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Interferon α-5 |
Drug: Interferon α-5
3 MIU or safe dose used three times a week (TIW) in alternate days in monotherapy. 29 days of treatment. Subcutaneous injection.
|
| Experimental: Interferon α-5 plus Interferon α-2b |
Drug: Interferon-α5 plus Interferon-α 2b
Interferon-α5 plus Interferon-α 2b. 1.5 MIU each, or safe dose used TIW in alternate days in combined therapy. 29 days of treatment. Subcutaneous injection.
|
| Active Comparator: Interferon α-2b (INTRON® A) |
Drug: Interferon α-2b (INTRON® A)
3 million IU TIW in alternate days in monotherapy. 29 days of treatment. Subcutaneous injection.
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Patients aged ≥18 years old,
- With chronic hepatitis C (CHC) infection diagnosed by seropositivity for anti-HCV antibodies or detectable HCV-RNA, at least 6 months prior to screening.
- Patients with CHC infection of genotype 1 (1a, 1b or mixed 1a/1b)
- Defined as relapsers: those CHC patients who had achieved virologic response (HCV-RNA non detectable) at any time during the standard care of treatment for CHC with IFN-α2 or PegIFN-α2 + ribavirin, and maintained it trough the end of treatment at week 48 weeks, but HCV-RNA detection occurs before 6 months post-treatment.
- In whom liver cirrhosis has been ruled out through fibro-scan or liver biopsy within 24 months prior to study enrolment.
- With a serum HCV viral load ≥ 100.000 IU/mL at screening
- With alanine-aminotransferase (ALT) and aspartate-aminotransferase (AST) serum measurements at screening less than 5 times of their upper limits of normal (ULN)
- With a body mass index (BMI) of at least 18 kg/m2, but not exceeding 36 kg/m2.
- For female subjects with childbearing potential: use of a known highly effective method of birth control
- For male subjects with partners of child bearing potential: use of appropriate contraceptive methods.
- Is able to effectively communicate with the investigator and other testing center personnel.
- Is able to participate and willing to give written informed consent and comply with the study restrictions.
Exclusion Criteria(principal):
- Hepatitis C infection of genotype 2, 3 or 4 or any mixed genotype (1/2, 1/3 and 1/4).
- A positive ELISA for HIV-1 or HIV-2.
- Hepatitis B virus (HBV) infection based on the presence of HBsAg.
- Hepatitis A virus (HAV) infection based on the presence of antiHAV-IgM. (AM 4)Criteria deleted
- Decompensated liver disease, or history of decompensated liver disease.
- History or other evidence of a medical condition associated with decompensated renal, immunologically mediated, chronic pulmonary, cardiac, thyroid, severe retinopathy, severe psychiatric, organ transplantation, cancer, seizure disorder or pancreatitis diseases.
- An active or suspected malignancy or history of malignancy within the last five years.
- Patients with a documented drug and alcohol addiction free history of at least 12 months who are, in the opinion of the investigator unlikely to relapse, may be enrolled in the study.
- Positive results for drug abuse at screening.Occasional use of cannabis previously to randomization is not an exclusion criteria -under investigator team criteria-. The patient should be advised of abstinence during the trial (AM 6)
- Haemoglobin <12.0g/dL for women, and <13.0g/dL for men at screening.
- White blood cell count <2000 cells/mm3 at screening.
- Absolute neutrophil count <1500 cells/mm3 at screening.
- Platelet count <100.000 cells/mm3 at screening.
- ALT and AST levels ≥ 5 xULN at screening.
- Prothrombin time INR prolonged to 1.5xULN at screening.
- TSH an T4 outside normal limits and not adequately controlled thyroid function at screening.
- Poorly controlled diabetes mellitus as evidenced by HbA1c >7.5% at screening.
- Alfa-fetoprotein value >100ng/mL at screening.
- Total bilirubin >1.5xULN with ratio of direct/indirect >1, at screening unless predominantly conjugated and reflecting Gilbert's disease
- Estimated creatinine clearance of 30 mL/minute or less at screening.
- Women who are confirmed to be pregnant
- People with known hypersensitivity to any ingredient of the investigational agents
- Patients who are at risk of bleeding.
- Haemoglobinopathy
- Screening ECG QTc value ≥ 450ms and/or clinically significant ECG findings.
- History of clinically significant drug allergies.
- Participation in a clinical study with an investigational drug, biologic, or device within 3 months prior to anticipated dose administration.
- Any chronic viral (including HSV), bacterial, mycobacterial, fungal, parasitic, or protozoal infection.
- Requirement for chronic systemic corticosteroids.
- Receiving systemic antivirals, hematopoietic growth factor, or immunomodulatory treatment within 30 days prior to enrollment.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01121731
Locations
| Spain | |
| Centre 013 | |
| A Coruña, Spain | |
| Centre 005 | |
| Barcelona, Spain | |
| Centre 004 | |
| Barcelona, Spain | |
| Centre 008 | |
| Barcelona, Spain | |
| Centre 011 | |
| Barcelona, Spain | |
| Centre 014 | |
| Granada, Spain | |
| Centre 015 | |
| León, Spain | |
| Centre 003 | |
| Madrid, Spain | |
| Centre 006 | |
| Madrid, Spain | |
| Centre 009 | |
| Madrid, Spain | |
| Centre 002 | |
| Madrid, Spain | |
| Centre 016 | |
| Madrid, Spain | |
| Centre 001 | |
| Pamplona, Spain | |
| Centre 012 | |
| Santander, Spain | |
| Centre 010 | |
| Sevilla, Spain | |
Sponsors and Collaborators
Digna Biotech S.L.
Investigators
| Principal Investigator: | Jesús Prieto, MD, PhD | Clínica Universidad de Navarra. Spain |
More Information
No publications provided
| Responsible Party: | Digna Biotech S.L. |
| ClinicalTrials.gov Identifier: | NCT01121731 History of Changes |
| Other Study ID Numbers: | NAHE001-CHC-01, 2009-012924-10 |
| Study First Received: | May 10, 2010 |
| Last Updated: | February 4, 2013 |
| Health Authority: | Spain: Agencia Española de Medicamentos y Productos Sanitarios |
Keywords provided by Digna Biotech S.L.:
|
Chronic Hepatitis C Viral Infection Interferon alfa-5 Interferon |
Additional relevant MeSH terms:
|
Hepatitis Hepatitis A Hepatitis, Chronic Hepatitis C Virus Diseases Hepatitis C, Chronic Liver Diseases Digestive System Diseases Hepatitis, Viral, Human Enterovirus Infections Picornaviridae Infections RNA Virus Infections Flaviviridae Infections Interferon-alpha Interferon Alfa-2a |
Interferon Alfa-2b Interferons Reaferon Antiviral Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Immunologic Factors Physiological Effects of Drugs Angiogenesis Inhibitors Angiogenesis Modulating Agents Growth Substances Growth Inhibitors Antineoplastic Agents Adjuvants, Immunologic |
ClinicalTrials.gov processed this record on May 21, 2013