A Bioequivalence Study of Pegylated Interferon Alfa-2a (PEG-IFN Alfa-2a) Benzyl Alcohol (BA)-Free Formulation Versus PEG-IFN Alfa-2a (Pegasys) Following Subcutaneous Administration
Study Details
Study Description
Brief Summary
This is an open-label, randomized, multi-center, single dose, two-period, two-sequence crossover study to investigate the bioequivalence of PEG-IFN alfa-2a BA-free formulation versus the reference market formulation (PEG-IFN alfa-2a [Pegasys®]) following subcutaneous administration via prefilled syringe in healthy Chinese participants.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Test Followed by Reference Participants will receive PEG-IFN alfa-2a BA-free formulation (Test) in Period 1, followed by PEG-IFN alfa-2a market formulation (Reference) in Period 2 on Day 1 of each period with a washout period of 14 to 21 days. |
Drug: PEG-IFN alfa-2a BA-free formulation (Test)
Participants will receive single injection of 180 micrograms (mcg) of PEG-IFN alfa-2a BA-free formulation, subcutaneously via prefilled syringe in either period 1 and 2 (each period having 35 days).
Drug: PEG-IFN alfa-2a market formulation (Reference)
Participants will receive single injection of 180 mcg of PEG-IFN alfa-2a market formulation, subcutaneously via prefilled syringe in either period 1 and 2 (each period having 35 days).
Other Names:
|
| Experimental: Reference Followed by Test Participants will receive PEG-IFN alfa-2a market formulation (Reference) in Period 1, followed by PEG-IFN alfa-2a BA-free formulation (Test) in Period 2 on Day 1 of each period with a washout period of 14 to 21 days. |
Drug: PEG-IFN alfa-2a BA-free formulation (Test)
Participants will receive single injection of 180 micrograms (mcg) of PEG-IFN alfa-2a BA-free formulation, subcutaneously via prefilled syringe in either period 1 and 2 (each period having 35 days).
Drug: PEG-IFN alfa-2a market formulation (Reference)
Participants will receive single injection of 180 mcg of PEG-IFN alfa-2a market formulation, subcutaneously via prefilled syringe in either period 1 and 2 (each period having 35 days).
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Maximum Observed Concentration (Cmax) for PEG-IFN alfa-2a [Predose (-1 Hour), Hour 1, 3, 5, 8, 12, 24, 48, 72, 84, 96, 120, 144, 168, 192, 216, 240, 312, 384, 480, 552, 648, 816 post Dose]
- Area Under the Concentration-Time Curve (AUC) for PEG-IFN alfa-2a From Time Zero to 816 hours (AUC0-816h) [Predose (-1 Hour), Hour 1, 3, 5, 8, 12, 24, 48, 72, 84, 96, 120, 144, 168, 192, 216, 240, 312, 384, 480, 552, 648, 816 post Dose]
Secondary Outcome Measures
- Area Under the Concentration-Time Curve for PEG-IFN alfa-2a From Time Zero Extrapolated to Infinity (AUC0-inf) [Predose (-1 Hour), Hour 1, 3, 5, 8, 12, 24, 48, 72, 84, 96, 120, 144, 168, 192, 216, 240, 312, 384, 480, 552, 648, 816 post Dose]
- Time to Reach Cmax (tmax) for PEG-IFN alfa-2a [Predose (-1 Hour), Hour 1, 3, 5, 8, 12, 24, 48, 72, 84, 96, 120, 144, 168, 192, 216, 240, 312, 384, 480, 552, 648, 816 post Dose]
- Terminal Half-Life (t1/2) for PEG-IFN alfa-2a [Predose (-1 Hour), Hour 1, 3, 5, 8, 12, 24, 48, 72, 84, 96, 120, 144, 168, 192, 216, 240, 312, 384, 480, 552, 648, 816 post Dose]
- Percentage of Participants With Adverse Events [Baseline up to 35 days post last dose of PEG-IFN alfa-2a (maximum up to 17.5 weeks)]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Healthy female and male Chinese participants
-
Body mass index between 19 and 28 kilograms per square meter (kg/m^2), inclusive
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Participants determined as healthy by their medical history, physical examination, vital signs, electrocardiogram (ECG), and clinical laboratory measurements performed at the Screening visit
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Female participants of childbearing potential: willing to use highly effective methods of contraception throughout the study and for 90 days after the last dosing
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Male participants: agreement to remain abstinent or use spermicide and barrier method contraception throughout the study and for 90 days after the last dosing
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Able to participate and willing to give written informed consent and to comply with the study restrictions
Exclusion Criteria:
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Any clinically relevant condition or history of cardiovascular, psychiatric, gastrointestinal, respiratory, renal, hepatic, hematological, lymphatic, neurological (including seizure history), musculoskeletal, genitourinary, immunological, metabolic, malignant, or dermatological disorder
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Participants who are positive for hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (anti HCV) or human immunodeficiency virus I and II antibody (anti-HIV I, anti-HIV II) tests at Screening
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Participants with alanine aminotransferase (ALT) above the upper limit of normal at Screening or on Day -1 of Period 1
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Any other condition or disease (other than those already stated) which, in the judgment of the Investigator, would place the participant at undue risk, interfere with the absorption, distribution, metabolism, and excretion of PEG-IFN alfa-2a, or interfere with the ability of the participant to complete the study
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History of drug or alcohol abuse within the last year before screening
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Treatment with interferon or PEG-IFN alfa-2a within 3 months prior to the first dosing
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Female participants who are pregnant, currently lactating, or have a positive serum pregnancy test at screening or have a positive urine pregnancy test on Day -1 of Period 1
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Use of any prescribed or over the counter medication or herbal medicine taken within 14 days prior to the first dosing or within 5 times the elimination half-life of the medication prior to the first dosing (whichever is longer). Exceptions are paracetamol, the contraceptive pill, hormone replacement therapy and commonly used vitamin supplements, which are permitted
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Regular smoking with consumption of more than 10 cigarettes per day or an equivalent amount of tobacco
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Participation in an investigational drug or device study within 3 months prior to the first dosing
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | CMAX A division of IDT Australia Limited | Adelaide | South Australia | Australia | 5000 |
| 2 | The University of Hong Kong; Pharmacy Clinical Trials | Hong Kong | Hong Kong | ||
| 3 | The Chinese University of Hong Kong; Emergency Medicine | Shatin | Hong Kong | 00000 | |
| 4 | Christchurch Clinical Studies Trust | Christchurch | New Zealand | 8011 | |
| 5 | Auckland Clinical Studies Limited | Grafton | New Zealand | 1010 | |
| 6 | SingHealth Investigational Medicine Unit; Haematology | Singapore | Singapore | 169608 | |
| 7 | Changi General Hospital- Parent; Department of Rheumatology | Singapore | Singapore | 529889 | |
| 8 | China Medical University Hospital;Oncology and Hematology Office Critical Care Center, 14H | Taichung | Taiwan | 404 | |
| 9 | Taipei Medical University Hospital; Clinical Research Center | Taipei City | Taiwan | 110 |
Sponsors and Collaborators
- Hoffmann-La Roche
Investigators
- Study Director: Clinical Trials, Hoffmann-La Roche
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- YV29573