Hepatitis BPhase 1NCT03032536
Study of the Relative Oral Bioavailability of AL-3778 Tablets and Drug Interaction With Entecavir or Tenofovir Disoproxil Fumarate in Healthy Volunteers
A Phase 1 study testing AL-3778, Entecavir and Tenofovir disoproxil fumarate in people with Hepatitis B and Chronic Hepatitis B, run by Alios Biopharma Inc. at 2 sites in New Zealand.
Trial summary
This is an open-label, randomized, multi-part study to evaluate the relative oral bioavailability of a tablet formulation of AL-3778 (formerly NVR 3-778) administered under fasted and fed conditions (Parts 1 and 2) and the drug-drug interaction between AL-3778 and entecavir or tenofovir disoproxil fumarate (Part 3). Read more about this study
- Who is it for?
- Ages 18 to 60 yearsHealthy volunteers can take part
- Conditions the study is for
- Hepatitis B, Chronic Hepatitis B, Viral Hepatitis B
- What is being tested?
- AL-3778, Entecavir and Tenofovir disoproxil fumarate
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 54 participants
- Where
- 2 sitesNew Zealand
- Study dates
- 31 Jan 2017to 28 Jun 2017
- Phase
- Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 60 years
- All sexes
- Healthy volunteers accepted
- Adult
Main Inclusion Criteria for All Subjects:
- Subject has provided written consent.
- In the investigator's opinion, the subject is able to understand and comply with protocol requirements, instructions, and study restrictions and is likely to complete the study as planned.
- Subject is in good health as deemed by the investigator, based on the totality of findings following a medical evaluation, including medical history, physical examination, laboratory tests and ECG.
- Male or female, 18-60 years of age.
- Body mass index 18-30 kg/m2, inclusive. The minimum weight is 50 kg.
- A female subject is eligible to participate in this study if she is of non-childbearing potential (defined as females with a documented tubal ligation, bilateral oophorectomy or hysterectomy) or postmenopausal (defined as 12 months of spontaneous amenorrhea and follicle stimulating hormone level within the laboratory's reference range for postmenopausal females). A post-menopausal female receiving hormone replacement therapy who is willing to discontinue hormone therapy 28 days before study drug dosing and agrees to remain off hormone replacement therapy for the duration of the study may be eligible for study participation.
- If male, subject is surgically sterile or practicing required forms of birth control until 6 months after the last dose of the study drug(s). Males must agree to refrain from sperm donation from check-in through 6 months after the last dose of the study drug(s).
- Subject has been a nonsmoker and has not used nicotine or nicotine-containing products for at least 6 months.
- Subjects who participated in Part 1 and/or Part 2 may participate in subsequent Part(s) upon satisfactory completion of a posttreatment visit, 7 days (+2 days) following the subject's last dose, and provided they continue to meet all of the inclusion criteria and none of the exclusion criteria.
Main exclusion criteria:
- Subject is mentally or legally incapacitated, has significant emotional problems at the time of prestudy (screening) visit or expected during the conduct of the study or has a history of a clinically significant psychiatric disorder over the last 5 to 10 years.
- Subject has a history of any illness that, in the opinion of the investigator, would confound the objectives or results of the study or poses an additional risk to the subject by their participation in the study.
- Subject has an estimated creatinine clearance of ≤80 mL/min based on the Cockcroft-Gault equation; An actual creatinine clearance, as determined by a 24-hour urine collection, may be used in place of, or in conjunction with, the Cockcroft-Gault equation; subjects who have an actual or estimated creatinine clearance within 10% of 80 mL/min may be enrolled in the study at the discretion of the investigator.
- Pregnant or nursing (lactating) females, confirmed by a positive human chorionic gonadotropin laboratory test or females contemplating pregnancy. Men whose female partners are pregnant or contemplating pregnancy from the date of screening until 6 months after their last dose of study drugs.
- Clinically significant cardiovascular, respiratory, skeletal, renal, gastrointestinal, hematologic, hepatic, immunological, neurologic, endocrine, genitourinary abnormalities or disease or any other medical illness as determined by the investigator or Sponsor's Medical Monitor.
- Subject has a history of malignancy except completely excised basal cell carcinoma or squamous cell carcinoma of the skin.
- Subject lacks or has poor peripheral venous access.
- Positive screening result for hepatitis B, hepatitis C and/or HIV serology.
- Any condition that, in the opinion of the investigator, would compromise the study's objectives or the well-being of the subject or prevent the subject from meeting the study requirements.
- Clinically significant abnormal ECG findings. Particularly, a history or family history of prolonged QT syndrome (eg, torsade de pointes) or sudden cardiac death.
- ECG with PR >200 ms, QRS >120 ms, QTcF >450 ms, as assessed by triplicate 12-lead ECG at the screening visit.
- Subject has had major surgery, or clinically significant blood loss or elective blood donation of significant volume (ie, >500 mL) within 60 days of first dose of study drug; >1 unit of plasma within 7 days of first dose of study drug.
- Abnormal heart rate, respiratory rate, temperature or blood pressure values outside of the normal range (evaluated in a semi-recumbent or recumbent position after 5 minutes of rest). One repeat measurement after an additional 5 minutes of rest is permitted.
- Evidence of active infection.
- Unwilling to abstain from alcohol for at least 48 hours prior to the start of dosing through the study completion visit.
- History of regular alcohol intake >7 units per week of alcohol for females and >14 units per week for males (one unit is defined as 10 g alcohol) within 3 months of the screening visit.
- The subject has a positive screening or Day -1 drugs of abuse screen.
- The use of concomitant medications, including prescription, over the counter medications, and herbal medications (such as St. John's Wort [Hypericum perforatum]) within 30 days prior to the first dose of study medication is excluded, unless approved by the Sponsor's Medical Monitor. Occasional use of ibuprofen/paracetamol/ acetaminophen is permitted.
- Subject has received an investigational drug (including investigational vaccines) or used an invasive investigational medical device within 90 days before the planned study drug.
- Subject has a history of significant multiple and/or severe allergies, or has had an anaphylactic reaction or significant intolerability to prescription or non-prescription drugs or food.
- Hypersensitivity to the active substances or to any of the excipients of AL-3778, entecavir or tenofovir disoproxil fumarate.
- Subject has known allergy to heparin or history of heparin-induced thrombocytopenia.
- Abnormal biochemistry or hematology laboratory results obtained at screening determined to be clinically significant by the Investigator. Screening ALT, AST, GGT, albumin, and total bilirubin must be within normal ranges. Creatine kinase >1.5 x ULN is exlusionary
- Unwillingness or inability to comply with the study protocol for any other reason.
Trial locations and contacts
2 sites in 1 country.
New Zealand2 sites
Auckland Clinical Studies
Auckland, 1010
Christchurch Clinical Studies Trust
Christchurch, 8011
About this study
Official title: A Randomized, Open-label, Multi-part Study of the Relative Oral Bioavailability of AL-3778 Tablets and Drug Interaction With Entecavir or Tenofovir Disoproxil Fumarate in Healthy Volunteers
This is an open-label, randomized, multi-part study to evaluate the relative oral bioavailability of a tablet formulation of AL-3778 (formerly NVR 3-778) administered under fasted and fed conditions (Parts 1 and 2) and the drug-drug interaction between AL-3778 and entecavir or tenofovir disoproxil fumarate (Part 3).
- Conditions
- Hepatitis B, Chronic Hepatitis B, Viral Hepatitis B
- Being tested
- AL-3778, Entecavir, Tenofovir disoproxil fumarate
- Medical subject headings
- Hepatitis B, Hepatitis B, Chronic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AL-3778Drug
Also called NVR 3-778, JNJ-63595948, ALS-003778
AL-3778 tablets or capsules
EntecavirDrug
Entecavir once daily for 14 days
Tenofovir disoproxil fumarateDrug
Also called Viread
Tenofovir disoproxil fumarate once daily for 14 days
| Study group | Role | What they receive |
|---|---|---|
| Treatments A, B, C | Experimental | Part 1: Cross-Over
* Treatment A: AL-3778 6 x 100-mg capsules (fasted) once.
* Treatment B: AL-3778 2 x 300-mg tablets (fasted) once
* Treatment C: AL-3778 2 x 300-mg tablets (high-fat meal) once. Receives: Drug: AL-3778 |
| Treatments D, E, F | Experimental | Part 2 (optional): Cross-Over
* Treatment D: AL-3778 2×300-mg tablets (fasted) once.
* Treatment E: AL-3778 tablet Dose (fasted) once. Dose will match Treatment F dose and will be:
* 1000mg: 2 x 500-mg OR
* 800mg: 1 x 300-mg + 1 x 500-mg OR
* 700mg: 1 x 200-mg + 1 x 500-mg
* Treatment F: AL-3778 tablet Dose (high-fat meal) once. Dose will match Treatment E dose and will be:
* 1000mg: 2 x 500-mg OR
* 800mg: 1 x 300-mg + 1 x 500-mg OR
* 700mg: 1 x 200-mg + 1 x 500-mg Receives: Drug: AL-3778 |
| Treatment G | Experimental | Part 3: AL-3778 twice daily administered under fasted conditions for 14 days.
Dose will be determined by Part 1 and/or Part 2 and will be one of the following tablet dosages:
* 600mg: 2 x 300-mg OR
* 1000mg: 2 x 500-mg OR
* 800mg: 1 x 300-mg + 1 x 500-mg OR
* 700mg: 1 x 200-mg + 1 x 500-mg Receives: Drug: AL-3778 |
| Treatment H | Active comparator | Part 3: Entecavir 0.5 mg once daily administered under fasted conditions for 14 days Receives: Drug: Entecavir |
| Treatment I | Experimental | Part 3: AL-3778 twice daily with entecavir 0.5 mg once daily both administered under fasted conditions for 14 days.
AL-3778 dose will be determined by Part 1 and/or Part 2 and will be one of the following tablet dosages:
* 600mg: 2 x 300-mg OR
* 1000mg: 2 x 500-mg OR
* 800mg: 1 x 300-mg + 1 x 500-mg OR
* 700mg: 1 x 200-mg + 1 x 500-mg Receives: Drug: AL-3778; Drug: Entecavir |
| Treatment J | Active comparator | Part 3: Tenofovir disoproxil fumarate 300 mg once daily administered under fasted conditions for 14 days Receives: Drug: Tenofovir disoproxil fumarate |
| Treatment K | Experimental | Part 3: AL-3778 twice daily and tenofovir disoproxil fumarate 300 mg once daily both administered under fasted conditions for 14 days.
AL-3778 dose will be determined by Part 1 and/or Part 2 and will be one of the following tablet dosages:
* 600mg: 2 x 300-mg OR
* 1000mg: 2 x 500-mg OR
* 800mg: 1 x 300-mg + 1 x 500-mg OR
* 700mg: 1 x 200-mg + 1 x 500-mg Receives: Drug: AL-3778; Drug: Tenofovir disoproxil fumarate |
What is being measured
The primary outcome is the main question the study is designed to answer.
AL-3778, entecavir, tenofovir: Maximum observed plasma concentration (Cmax)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Area under the plasma concentration-time curve from time 0 to last measurable concentration (AUClast)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Area under the plasma concentration-time curve from time 0 to extrapolated to infinity (AUC∞)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Maximum observed plasma concentration on Day 1 (Cmax. Day 1)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1
AL-3778, entecavir, tenofovir: Minimum observed plasma concentration on Day 1 (Cmin, Day 1)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1
AL-3778, entecavir, tenofovir: Area under the plasma concentration-time curve from time 0 to dosing interval on Day 1 (AUC0-Τ, Day 1)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1
AL-3778, entecavir, tenofovir: Minimum observed plasma concentration (C_min)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
Secondary outcomes (15)
AL-3778, entecavir, tenofovir: Predose plasma concentrations (C_0-h)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Last observed plasma concentration (C_last)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Time of the maximum observed plasma concentration (T_max)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Time to last measurable plasma concentration (T_last)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Apparent oral clearance (CL/F)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Apparent volume of distribution (Vz/F)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Apparent terminal half-life (t½)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Maximum observed plasma concentration on Day 14 (Cmax. Day 14)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 14
AL-3778, entecavir, tenofovir: Minimum observed plasma concentration on Day 14 (Cmin, Day 14)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 14
AL-3778, entecavir, tenofovir: Area under the plasma concentration-time curve from time 0 to dosing interval, tau, on Day 14 (AUC0-Τ, Day 14)
Measured: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14
Incidence, nature, and severity of adverse events
Measured: Screening to Day 22
Changes in Vital Signs during and after study drug administration
Measured: Day 1 to Day 22
changes in physical examinations during and after study drug administration
Measured: Day 1 to Day 22
changes in clinical laboratory results during and after study drug administration
Measured: Day 1 to Day 22
changes in electrocardiogram results during and after study drug administration
Measured: Day 1 to Day 22
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Jan 2017 (estimated)
- Study start31 Jan 2017
- Primary completion28 Jun 2017
- Study completion28 Jun 2017
Why it stopped: Sponsor decision.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hepatitis BStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 54 participants (actual)
Sponsor and investigators
- Lead sponsor
- Alios Biopharma Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- William D Kennedy, MD, Study director, Alios Biopharma Inc.
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03032536
- Sponsor's protocol ID
- AL-3778-1002
- Other IDs
- U1111-1187-4391
- Status last verified
- Oct 2017
- First submitted
- 24 Jan 2017
- Last updated
- 16 Oct 2017
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Yes: Data will be provided per regulatory requirements.
Study at a glance
From the registry record, last updated by the sponsor on 16 Oct 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized, Open-label, Multi-part Study of the Relative Oral Bioavailability of AL-3778 Tablets and Drug Interaction With Entecavir or Tenofovir Disoproxil Fumarate in Healthy Volunteers
- ClinicalTrials.gov ID
- NCT03032536
- Acronym / sponsor ID
- AL-3778-1002
- Conditions
- Hepatitis B, Chronic Hepatitis B, Viral Hepatitis B
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Sponsor decision.
- Enrolment
- 54 participants (actual)
- Lead sponsor
- Alios Biopharma Inc.Industry (pharma, biotech, devices)
- Study start
- 31 Jan 2017 (actual)
- Primary completion
- 28 Jun 2017 (actual)
- Study completion
- 28 Jun 2017 (actual)
- First posted
- 26 Jan 2017 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is an open-label, randomized, multi-part study to evaluate the relative oral bioavailability of a tablet formulation of AL-3778 (formerly NVR 3-778) administered under fasted and fed conditions (Parts 1 and 2) and the drug-drug interaction between AL-3778 and entecavir or tenofovir disoproxil fumarate (Part 3).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 7
| Arm | Type | Receives |
|---|---|---|
| Treatments A, B, C | Experimental | Drug: AL-3778Part 1: Cross-Over * Treatment A: AL-3778 6 x 100-mg capsules (fasted) once. * Treatment B: AL-3778 2 x 300-mg tablets (fasted) once * Treatment C: AL-3778 2 x 300-mg tablets (high-fat meal) once. |
| Treatments D, E, F | Experimental | Drug: AL-3778Part 2 (optional): Cross-Over * Treatment D: AL-3778 2×300-mg tablets (fasted) once. * Treatment E: AL-3778 tablet Dose (fasted) once. Dose will match Treatment F dose and will be: * 1000mg: 2 x 500-mg OR * 800mg: 1 x 300-mg + 1 x 500-mg OR * 700mg: 1 x 200-mg + 1 x 500-mg * Treatment F: AL-3778 tablet Dose (high-fat meal) once. Dose will match Treatment E dose and will be: * 1000mg: 2 x 500-mg OR * 800mg: 1 x 300-mg + 1 x 500-mg OR * 700mg: 1 x 200-mg + 1 x 500-mg |
| Treatment G | Experimental | Drug: AL-3778Part 3: AL-3778 twice daily administered under fasted conditions for 14 days. Dose will be determined by Part 1 and/or Part 2 and will be one of the following tablet dosages: * 600mg: 2 x 300-mg OR * 1000mg: 2 x 500-mg OR * 800mg: 1 x 300-mg + 1 x 500-mg OR * 700mg: 1 x 200-mg + 1 x 500-mg |
| Treatment H | Active comparator | Drug: EntecavirPart 3: Entecavir 0.5 mg once daily administered under fasted conditions for 14 days |
| Treatment I | Experimental | Drug: AL-3778, Drug: EntecavirPart 3: AL-3778 twice daily with entecavir 0.5 mg once daily both administered under fasted conditions for 14 days. AL-3778 dose will be determined by Part 1 and/or Part 2 and will be one of the following tablet dosages: * 600mg: 2 x 300-mg OR * 1000mg: 2 x 500-mg OR * 800mg: 1 x 300-mg + 1 x 500-mg OR * 700mg: 1 x 200-mg + 1 x 500-mg |
| Treatment J | Active comparator | Drug: Tenofovir disoproxil fumaratePart 3: Tenofovir disoproxil fumarate 300 mg once daily administered under fasted conditions for 14 days |
| Treatment K | Experimental | Drug: AL-3778, Drug: Tenofovir disoproxil fumaratePart 3: AL-3778 twice daily and tenofovir disoproxil fumarate 300 mg once daily both administered under fasted conditions for 14 days. AL-3778 dose will be determined by Part 1 and/or Part 2 and will be one of the following tablet dosages: * 600mg: 2 x 300-mg OR * 1000mg: 2 x 500-mg OR * 800mg: 1 x 300-mg + 1 x 500-mg OR * 700mg: 1 x 200-mg + 1 x 500-mg |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| AL-3778Also: NVR 3-778, JNJ-63595948, ALS-003778AL-3778 tablets or capsules | Drug | Treatment G, Treatment I, Treatment K, Treatments A, B, C, Treatments D, E, F |
| EntecavirEntecavir once daily for 14 days | Drug | Treatment H, Treatment I |
| Tenofovir disoproxil fumarateAlso: VireadTenofovir disoproxil fumarate once daily for 14 days | Drug | Treatment J, Treatment K |
Primary outcome
AL-3778, entecavir, tenofovir: Maximum observed plasma concentration (Cmax)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Area under the plasma concentration-time curve from time 0 to last measurable concentration (AUClast)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Area under the plasma concentration-time curve from time 0 to extrapolated to infinity (AUC∞)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Maximum observed plasma concentration on Day 1 (Cmax. Day 1)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1
AL-3778, entecavir, tenofovir: Minimum observed plasma concentration on Day 1 (Cmin, Day 1)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1
AL-3778, entecavir, tenofovir: Area under the plasma concentration-time curve from time 0 to dosing interval on Day 1 (AUC0-Τ, Day 1)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1
AL-3778, entecavir, tenofovir: Minimum observed plasma concentration (C_min)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
15 secondary outcomes
AL-3778, entecavir, tenofovir: Predose plasma concentrations (C_0-h)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Last observed plasma concentration (C_last)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Time of the maximum observed plasma concentration (T_max)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Time to last measurable plasma concentration (T_last)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Apparent oral clearance (CL/F)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Apparent volume of distribution (Vz/F)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Apparent terminal half-life (t½)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22
AL-3778, entecavir, tenofovir: Maximum observed plasma concentration on Day 14 (Cmax. Day 14)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 14
AL-3778, entecavir, tenofovir: Minimum observed plasma concentration on Day 14 (Cmin, Day 14)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 14
AL-3778, entecavir, tenofovir: Area under the plasma concentration-time curve from time 0 to dosing interval, tau, on Day 14 (AUC0-Τ, Day 14)
Time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14
Incidence, nature, and severity of adverse events
Time frame: Screening to Day 22
Changes in Vital Signs during and after study drug administration
Time frame: Day 1 to Day 22
changes in physical examinations during and after study drug administration
Time frame: Day 1 to Day 22
changes in clinical laboratory results during and after study drug administration
Time frame: Day 1 to Day 22
changes in electrocardiogram results during and after study drug administration
Time frame: Day 1 to Day 22
Results and safety
The study was stopped early (reason given: Sponsor decision.). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Oct 2017.
- Individual participant dataSharing planned: Yes. Data will be provided per regulatory requirements.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
William D Kennedy, MD study director
Alios Biopharma Inc.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing AL-3778, Entecavir and Tenofovir disoproxil fumarate in people with Hepatitis B and Chronic Hepatitis B, run by Alios Biopharma Inc. at 2 sites in New Zealand.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 16 Oct 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in New Zealand. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: Sponsor decision.). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
AL-3778, entecavir, tenofovir: Maximum observed plasma concentration (Cmax) (time frame: At 0, 0.5, 1, 2, 3, 4, 6, 8, 10, 12 hours after dosing on Day 1 and 14 and once per day on Day 8, 10, 12, and 22). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Oct 2017.