Chronic Hepatitis bPhase 2NCT04157257
An Study to Evaluate Safety and Efficacy of QL-007 Tablets in Combination With Entecavir or Tenofovir in Patients With Chronic Hepatitis b Who Have Received Nucleoside (Acid) Therapy
A Phase 2 study testing TDF tablet, Entecavir Tablet and QL-007 in people with Chronic Hepatitis b, run by Qilu Pharmaceutical Co., Ltd. at 2 sites in China.
Trial summary
This is an open label, randomized, multi-center, comparative study. Subjects will be screened prior to study entry to establish eligibility. 60 Subjects who meet all the selection criteria will be randomly assigned to (A) QL007 200mg BID+ Tenofovir dipirofurate fumarate (TDF)300 mg QD, (B) QL007 200 mg BID+ Entecavir… Read more about this study
- Who is it for?
- Ages 18 to 70 years
- Conditions the study is for
- Chronic Hepatitis b
- What is being tested?
- TDF tablet, Entecavir Tablet and QL-007
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 2 sitesChina
- Study dates
- 26 Jul 2019to Oct 2022
- Phase
- Phase 2
- 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 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients aged 18-70 years (inclusive) with chronic HBV infection prior to baseline;
- Subjects who have received a entecavir or tenofovir ester treatment for more than 1 year before screening ;
- HBsAg > 250 IU/mL and HBV DNA < 60 IU/mL at screening period;
- ALT≤ 2×ULN;
- Participants must have understood and signed the ICF.
Who cannot join
- Confirmed co-infection with human immunodeficiency virus (HIV), hepatitis C virus (HCV) or hepatitis D virus (HDV);
- History of liver disease other than chronic hepatitis B;
- History of Gilbert's Disease;
- History of decompensated liver disease or any sign of decompensated liver disease at the screening period;
- Evidence of moderate or severe fibrosis or cirrhosis;
- Evidence of HCC or AFP > 50 ng/ml at the screening period.
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- Any Clinical laboratory values meet the certain standards at the screening period;
- Subjects have clinically significant, uncontrolled heart disease and/or recent cardiac event;
- Risks of serious kidney and respiratory diseases;
- Impaired gastrointestinal (GI) function or GI disease that may alter absorption of QL-007 as determined by the Investigator;
- Receiving medications that meet one of the following criteria and that cannot be discontinued ≥1 week prior to the start of treatment QL-007:
- Medication with a known risk of prolonging the QT interval or inducing Torsades de Pointes;
- Moderate or strong inhibitors or strong inducers of CYP3A4
- Intake of any drugs that can reduce enzyme activity;
- History of bleeding diathesis;
- Risks of mental and nervous system diseases during screening;
- Pregnant or lactating female subjects; Female subjects of childbearing age who were not willing to use effective contraception throughout the study period or male subjects whose partners were fertile but were not willing to use effective contraception;
- Volunteers who took an Investigational Product within 3 months or who have been within 5 half-lives of other trial drugs before the randomization;
- Any other condition , which in the opinion of investigator would make a patient unfit for participation in a clinical study.
Trial locations and contacts
2 sites in 1 country.
China2 sites, 2 recruiting
- Recruiting
The first hospital of jilin university
Changchun, Jilin, 130000
Junqi Niu, PhD
- Recruiting
Southern Hospital of Southern Medical University
Guangzhou, Guangdong, 510000
Jinlin Hou, PhD
About this study
Official title: An Open-Label Phase 2 Study to Evaluate Safety and Efficacy of QL-007 Tablets in Combination With Entecavir or Tenofovir in Patients With Chronic Hepatitis b Who Have Received Nucleoside (Acid) Therapy : a Multicenter, Randomized, Positive Controlled Clinical Trialcontrolled Clinical Trial
This is an open label, randomized, multi-center, comparative study. Subjects will be screened prior to study entry to establish eligibility. 60 Subjects who meet all the selection criteria will be randomly assigned to (A) QL007 200mg BID+ Tenofovir dipirofurate fumarate (TDF)300 mg QD, (B) QL007 200 mg BID+ Entecavir 0.5 mg QD, (C)TDF 300 mg QD, (D) Entecavir 0.5 mg QD.
The purpose of this study was to evaluate the efficacy and safety of QL-007 tables in combination with TDF or Entecavir in patients with chronic hepatitis b who have received nucleoside (acid) therapy, and to recommend a reasonable regimen for phase III study.
Read the detailed description
The subjects received the drug treatment for a maximum of 96 weeks: divided into two stages: the first stage: 0-24 weeks as the core treatment period, 25-48 weeks as the extended treatment period. The second stage: 49-96 weeks is the extended treatment period. Stage 2: subjects in stage 1 group A and C were grouped into group E(QL-007 200 mg BID或XX mg +TDF 300 mg QD), and subjects in group B and D were grouped into group F(QL-007 200 mg BID或XX mg + Entecavir 0.5 mg QD). Subjects in group E and F entered the second stage of treatment according to 200 mg BID. After the efficacy data of the original treatment clinical trial (protocol 201) determine the optimal dose of 007, all subjects entering the second phase will receive the optimal dose of 007 and continue treatment withTDF or Entecavir tablets (007 XXmg+TDF or ETV) into the second phase 49-96 weeks of extended treatment.
- Conditions
- Chronic Hepatitis b
- Being tested
- TDF tablet, Entecavir Tablet, QL-007
- Keywords
- nucleoside (acid) therapy
- Medical subject headings
- Hepatitis B, Chronic, Heartburn
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
TDF tabletDrug
Also called Tenofovir dipirofurate fumarate tablet
TDF tablet 300mg QD
Entecavir TabletDrug
Also called Entecavir
Entecavir tablet 0.5mg QD
QL-007Drug
Also called QL-007 tablet
QL-007 tablets 200mg BID
| Study group | Role | What they receive |
|---|---|---|
| QL-007 +TDF | Experimental | QL-007 200 mg BID +TDF 300 mg QD Receives: Drug: TDF tablet; Drug: QL-007 |
| QL-007 +Entecavir | Experimental | QL-007 200 mg BID +Entecavir 0.5 mg QD Receives: Drug: Entecavir Tablet; Drug: QL-007 |
| TDF monotherapy | Active comparator | TDF tablet 300 mg QD Receives: Drug: TDF tablet |
| Entecavir monotherapy | Active comparator | Entecavir tablet 0.5 mg QD Receives: Drug: Entecavir Tablet |
What is being measured
The primary outcome is the main question the study is designed to answer.
Main index of pharmacodynamics
The change of HBsAg levels at week 24 compared to baseline
Measured: 24 weeks
Secondary outcomes (5)
The secondary pharmacodynamic index
The changes of HBsAg and HBeAg level at week 4, 8, 12, 16, 20, 24, 36, 48, 60, 72, 84, 96 compared to baseline
Measured: 96 weeks
The secondary pharmacodynamic index
The percentage of subjects with HBsAg and HBeAg serological clearance and/or seroconversion at 4, 8, 12, 16, 20, 24, 36, 48, 60, 72, 84, 96 weeks
Measured: 96 weeks
The secondary pharmacodynamic index
The percentage of subjects with normal ALT level at weeks 4, 8, 12, 16, 20, 24, 36, 48, 60, 72, 84 and 96
Measured: 96 weeks
Other evaluation indexes of pharmacodynamics exploration
The changes of HBV RNA and HBcrAg compared with baseline at week 4, 8, 12, 16, 20, 24, 36, 48, 60, 72, 84 and 96
Measured: 96 weeks
To evaluate the safety of QL-007 in combination with TDF or Entecavir: incidence of adverse events
The incidence of adverse events
Measured: 96 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Nov 2019
- Study start26 Jul 2019
- Primary completionDec 2020 (estimated)
- Study completionOct 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Hepatitis bStudies of the same condition, open and under way.
- More trials run by Qilu Pharmaceutical Co., Ltd.The sponsor's other registered studies.
- 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 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Qilu Pharmaceutical Co., Ltd.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Jinlin Hou, PhD, Principal investigator, Southern Hospital of Southern Medical UniversityJunqi Niu, PhD, Principal investigator, The First Hospital of Jilin University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04157257
- Sponsor's protocol ID
- QL-007-202
- Status last verified
- Nov 2019
- First submitted
- 6 Nov 2019
- Last updated
- 8 Nov 2019
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 8 Nov 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Open-Label Phase 2 Study to Evaluate Safety and Efficacy of QL-007 Tablets in Combination With Entecavir or Tenofovir in Patients With Chronic Hepatitis b Who Have Received Nucleoside (Acid) Therapy : a Multicenter, Randomized, Positive Controlled Clinical Trialcontrolled Clinical Trial
- ClinicalTrials.gov ID
- NCT04157257
- Acronym / sponsor ID
- QL-007-202
- Conditions
- Chronic Hepatitis b
- Keywords
- nucleoside (acid) therapy
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Qilu Pharmaceutical Co., Ltd.Industry (pharma, biotech, devices)
- Study start
- 26 Jul 2019 (actual)
- Primary completion
- Dec 2020 (estimated)
- Study completion
- Oct 2022 (estimated)
- First posted
- 8 Nov 2019 (actual)
- 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-center, comparative study. Subjects will be screened prior to study entry to establish eligibility. 60 Subjects who meet all the selection criteria will be randomly assigned to (A) QL007 200mg BID+ Tenofovir dipirofurate fumarate (TDF)300 mg QD, (B) QL007 200 mg BID+ Entecavir 0.5 mg QD, (C)TDF 300 mg QD, (D) Entecavir 0.5 mg QD.
The purpose of this study was to evaluate the efficacy and safety of QL-007 tables in combination with TDF or Entecavir in patients with chronic hepatitis b who have received nucleoside (acid) therapy, and to recommend a reasonable regimen for phase III study.
Detailed description
The subjects received the drug treatment for a maximum of 96 weeks: divided into two stages: the first stage: 0-24 weeks as the core treatment period, 25-48 weeks as the extended treatment period. The second stage: 49-96 weeks is the extended treatment period. Stage 2: subjects in stage 1 group A and C were grouped into group E(QL-007 200 mg BID或XX mg +TDF 300 mg QD), and subjects in group B and D were grouped into group F(QL-007 200 mg BID或XX mg + Entecavir 0.5 mg QD). Subjects in group E and F entered the second stage of treatment according to 200 mg BID. After the efficacy data of the original treatment clinical trial (protocol 201) determine the optimal dose of 007, all subjects entering the second phase will receive the optimal dose of 007 and continue treatment withTDF or Entecavir tablets (007 XXmg+TDF or ETV) into the second phase 49-96 weeks of extended treatment.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| QL-007 +TDF | Experimental | Drug: TDF tablet, Drug: QL-007QL-007 200 mg BID +TDF 300 mg QD |
| QL-007 +Entecavir | Experimental | Drug: Entecavir Tablet, Drug: QL-007QL-007 200 mg BID +Entecavir 0.5 mg QD |
| TDF monotherapy | Active comparator | Drug: TDF tabletTDF tablet 300 mg QD |
| Entecavir monotherapy | Active comparator | Drug: Entecavir TabletEntecavir tablet 0.5 mg QD |
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Patients aged 18-70 years (inclusive) with chronic HBV infection prior to baseline;
- Subjects who have received a entecavir or tenofovir ester treatment for more than 1 year before screening ;
- HBsAg > 250 IU/mL and HBV DNA < 60 IU/mL at screening period;
- ALT≤ 2×ULN;
- Participants must have understood and signed the ICF.
Key exclusion criteria (19 listed)
- Confirmed co-infection with human immunodeficiency virus (HIV), hepatitis C virus (HCV) or hepatitis D virus (HDV);
- History of liver disease other than chronic hepatitis B;
- History of Gilbert's Disease;
- History of decompensated liver disease or any sign of decompensated liver disease at the screening period;
- Evidence of moderate or severe fibrosis or cirrhosis;
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 |
|---|---|---|
| TDF tabletAlso: Tenofovir dipirofurate fumarate tabletTDF tablet 300mg QD | Drug | QL-007 +TDF, TDF monotherapy |
| Entecavir TabletAlso: EntecavirEntecavir tablet 0.5mg QD | Drug | Entecavir monotherapy, QL-007 +Entecavir |
| QL-007Also: QL-007 tabletQL-007 tablets 200mg BID | Drug | QL-007 +Entecavir, QL-007 +TDF |
Primary outcome
Main index of pharmacodynamics
Time frame: 24 weeks
The change of HBsAg levels at week 24 compared to baseline
5 secondary outcomes
The secondary pharmacodynamic index
Time frame: 96 weeks
The secondary pharmacodynamic index
Time frame: 96 weeks
The secondary pharmacodynamic index
Time frame: 96 weeks
Other evaluation indexes of pharmacodynamics exploration
Time frame: 96 weeks
To evaluate the safety of QL-007 in combination with TDF or Entecavir: incidence of adverse events
Time frame: 96 weeks
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Nov 2019.
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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.
Jinlin Hou, PhD principal investigator
Southern Hospital of Southern Medical University
Junqi Niu, PhD principal investigator
The First Hospital of Jilin University
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing TDF tablet, Entecavir Tablet and QL-007 in people with Chronic Hepatitis b, run by Qilu Pharmaceutical Co., Ltd. at 2 sites in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 19 exclusion criteria. 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: status not confirmed, as of the sponsor's last update on 8 Nov 2019. 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 China. 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 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Anbo Xiang, PhD (18815317378, anbo.xiang@qilu-pharma.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Main index of pharmacodynamics (time frame: 24 weeks). 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 8 Nov 2019.