Normal Healthy VolunteerPhase 1NCT07140055
A Research Study to Evaluate BLX-7006 in Healthy Adults
A Phase 1 study testing BLX-7006 in people with Normal Healthy Volunteer and Safety After Oral Intake, run by Biolexis Therapeutics at 1 site in Australia.
Trial summary
This study will test an oral medicine called BLX-7006, which acts like the hormone Glucagon-like Peptide-1 (GLP-1) to help control blood sugar and body weight. Current GLP-1 medicines are given by injection. Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Normal Healthy Volunteer, Safety After Oral Intake
- What is being tested?
- BLX-7006
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 76 participants
- Where
- 1 siteAustralia
- Study dates
- Sep 2025to May 2026
- Phase
- Phase 1
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 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Healthy males or females, 18-65 years, BMI 20-35 kilograms/meter² (kg/m²), weight ≥50 kilograms (kg).
- Normal or clinically acceptable labs, vital signs
- HbA1c <6.5%, non-fasting glucose 4.0-7.8 milimol/Liter (mmol/L)
- Willing to follow contraception requirements, avoid alcohol, nicotine, and blood donation per protocol, and comply with all study visits and procedures.
Who cannot join
- History of diabetes, clinically significant cardiovascular, hepatic, renal, gastrointestinal, psychiatric, or neurologic disease, or abnormal labs/Echocardiograms (ECG) deemed clinically relevant.
- Prior gastrointestinal (GI) surgery affecting absorption (e.g., gastric bypass) or chronic GI disorders.
- History or family history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia type 2 (MEN2); malignancy within 5 years (except treated basal cell or in situ cervical cancer).
- History of severe allergic reactions, seizures, or psychiatric hospitalization; positive drug, alcohol, or cotinine test.
- Use of prescription drugs, Over the counter (OTC) /herbal supplements
- Participation in another clinical trial or blood donation within 30 days (or 5 half-lives of prior drug).
- Any condition or history that may compromise safety, study conduct, or compliance, in the opinion of the Investigator.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Australia1 site
Nucleus Network Brisbane Clinic
Brisbane, Queensland
(07) 3707 2720
About this study
Official title: A Phase 1 Randomized, Double-blind, Placebo-controlled Single-ascending Dose and Multiple-ascending Dose (SAD and MAD) Trial to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of the Novel Glucagon-like Peptide-1 Receptor Agonist (GLP-1RA) BLX-7006 in Healthy Adults With a Body Mass Index (BMI) of 20 - 35 kg/m2
This study will test an oral medicine called BLX-7006, which acts like the hormone Glucagon-like Peptide-1 (GLP-1) to help control blood sugar and body weight. Current GLP-1 medicines are given by injection. This study will see if BLX-7006 is safe, how the body processes it, and whether food changes how it is absorbed. The main goal is to see if BLX-7006 is safe and well tolerated. Secondary objectives of the study will measure how BLX-7006 moves through the body after an oral dose, including how quickly it is absorbed, how long it stays in the blood, and how the body removes it. It will also look at how the drug affects the body by looking at markers of glucose metabolism.
Read the detailed description
This is a Phase 1, single-center, first-in-human study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and the effect of food on the PK of BLX-7006, a novel oral small-molecule GLP-1 receptor agonist, in healthy adult volunteers. The study consists of three parts: single ascending dose (SAD), food effect (FE), and multiple ascending dose (MAD) assessments.
Study Rationale and Objectives:
BLX-7006 is being developed as an oral alternative to currently available injectable GLP-1 receptor agonists used for the treatment of metabolic diseases such as type 2 diabetes mellitus and obesity. Oral delivery of BLX-7006 may improve convenience and treatment adherence while maintaining the metabolic benefits of GLP-1 agonism. This Phase 1 study is designed to characterize the initial safety profile, define the PK properties of BLX-7006, evaluate preliminary PD biomarkers of glucose metabolism, and determine the impact of a high-fat meal on drug absorption.
Study Design Overview:
The study will enroll approximately 76 healthy adults across three sequential parts.
Part 1: Single Ascending Dose (SAD) This is a randomized, double-blind, placebo-controlled, sequential SAD study in up to four cohorts (approximately 8 participants per cohort; 6 active, 2 placebo). Doses will escalate sequentially following review of blinded safety, tolerability, PK, and PD data by a Safety Review Committee (SRC). A sentinel dosing approach will be used for each cohort (1 active, 1 placebo) prior to dosing the remainder of the cohort. Participants will be confined in the clinical research unit (CRU) for approximately 4 days for safety monitoring, PK and PD blood sampling, and will return for an end-of-study (EOS) visit on Day 8. SAD data will inform dose selection for the FE and MAD parts of the study.
Part 2: Food Effect (FE) This is an open-label, randomized, 2-period, 2-sequence crossover study designed to evaluate the effect of a high-fat, high-calorie meal on the PK of a single oral dose of BLX-7006. A single cohort of 12 participants will receive BLX-7006 under both fasted and fed conditions, with a 7-day washout between doses. Participants will be confined for approximately 4 days in each period, with safety, PK, and PD assessments performed throughout. The SRC may adjust the washout interval or timing of assessments based on PK results from the SAD cohorts to ensure adequate elimination between periods.
Part 3: Multiple Ascending Dose (MAD) This is a randomized, double-blind, placebo-controlled, sequential MAD study in up to four cohorts (approximately 8 participants per cohort; 6 active, 2 placebo). Participants will receive BLX-7006 or placebo orally once daily for 7 days. Participants will be confined from Day -1 through approximately Day 10 for dosing, safety assessments, and PK/PD sampling, with an EOS visit on Day 14. Dose escalation to subsequent MAD cohorts will occur following review of blinded safety, PK, and PD data by the SRC.
Safety Monitoring:
Safety will be evaluated throughout the study by monitoring adverse events (AEs), clinical laboratory tests, vital signs, 12-lead electrocardiograms (ECGs), and physical examinations. Sentinel dosing and SRC reviews between cohorts are incorporated to minimize risk.
Pharmacokinetic and Pharmacodynamic Assessments:
Blood samples will be collected to characterize single- and multiple-dose PK parameters of BLX-7006, including maximum concentration (Cmax), time to maximum concentration (Tmax), area under the curve (AUC), half-life (t½), and apparent clearance. PD endpoints will include biomarkers of glucose metabolism and insulin production. The FE part will compare PK parameters between fasted and fed states.
Dose Escalation and Cohort Progression:
The SRC will review cumulative safety, tolerability, PK, and PD data after each cohort before escalating to the next dose level. The number of cohorts may be reduced based on emerging data. The FE and MAD parts may proceed in parallel with later SAD cohorts once predefined safety criteria are met.
The results of this study will provide the initial clinical safety and PK/PD profile of BLX-7006, including preliminary assessment of food effect, to support future clinical development in populations with metabolic diseases.
- Conditions
- Normal Healthy Volunteer, Safety After Oral Intake
- Being tested
- BLX-7006, Placebo
- Keywords
- Obesity, Type 2 Diabetes, Metabolic Disorders, Normal Healthy Volunteer
- Medical subject headings
- Obesity, Diabetes Mellitus, Type 2, Metabolic Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BLX-7006Drug
BLX-7006 Single or Multiple doses administered orally as a tablet
PlaceboDrug
Participants will receive matching placebo of BLX-7006 for each of the oral cohorts.
| Study group | Role | What they receive |
|---|---|---|
| BLX-7006 Oral Dose | Experimental | Participants will receive oral BLX-7006 as a single dose (in Part 1 or 2) or once daily for 7 days (in Part 3). Receives: Drug: BLX-7006 |
| Placebo to match BLX-7006 | Placebo comparator | Participants will receive an oral placebo that looks like BLX-7006 but does not contain active drug as a single dose (in Part 1 or 2) or once daily for 7 days (in Part 3). Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of participants who experienced Adverse Events (AEs)
The safety and tolerability of oral BLX-7006 administration will be evaluated based on the incidence of adverse effects in subjects, as assessed according to CTCAE v5.0. The number of participants who experience an AE will be reported.
Measured: From first dose through End of Study (up to ~28 days per participant)
Number of participants who experienced Serious Adverse Events (SAEs)
The safety and tolerability of oral BLX-7006 administration will be evaluated based on the incidence of SAE in subjects, as assessed according to CTCAE v5.0. The number of participants who experience a SAE will be reported.
Measured: From first dose through End of Study (up to ~28 days per participant)
Number of participants who experienced Treatment-Related Adverse Avents (TRAEs)
The safety and tolerability of oral BLX-7006 administration will be evaluated based on the incidence of TRAEs in subjects, as assessed according to CTCAE v5.0. The number of participants who experience a TRAE will be reported.
Measured: From first dose through End of Study (up to ~28 days per participant)
Secondary outcomes (9)
Assess maximum observed drug concentration (Cmax)
Evaluate the relative bioavailability of BLX-7006 in single, food effect, and multiple ascending doses in healthy adults
Measured: Up to 14 days after last dose in each cohort
Assess time to maximum concentration (Tmax)
Evaluate the relative bioavailability of BLX-7006 in single, food effect, and multiple ascending doses in healthy adults
Measured: Up to 14 days after last dose in each cohort
Assess the area under the concentration-time curve from time 0 to infinity (AUCinf)
Evaluate the relative bioavailability of BLX-7006 in single, food effect, and multiple ascending doses in healthy adults
Measured: Up to 14 days after last dose in each cohort
Assess the area under the concentration curve from time 0 to the last quantifiable concentration (AUClast)
Evaluate the relative bioavailability of BLX-7006 in single, food effect, and multiple ascending doses in healthy adults
Measured: Up to 14 days after last dose in each cohort
Assess half-life (t½) plasma concentration
Evaluate the relative bioavailability of BLX-7006 in single, food effect, and multiple ascending doses in healthy adults
Measured: Up to 14 days after last dose in each cohort
Serum fructosamine levels
Evaluate the effect of single and multiple oral doses of BLX-7006 on serum fructosamine levels
Measured: Up to 14 days after last dose in each cohort
Insulin levels
Evaluate the effect of single and multiple oral doses of BLX-7006 on insulin levels
Measured: Up to 14 days after last dose in each cohort
C-peptide levels
Evaluate the effect of single and multiple oral doses of BLX-7006 on C-peptide levels
Measured: Up to 14 days after last dose in each cohort
Glucagon levels
Evaluate the effect of single and multiple oral doses of BLX-7006 on glucagon levels
Measured: Up to 14 days after last dose in each cohort]
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Aug 2025
- Study startSep 2025 (estimated)
- Primary completionApr 2026 (estimated)
- Study completionMay 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Normal Healthy VolunteerStudies 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
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 76 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Biolexis Therapeutics
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07140055
- Sponsor's protocol ID
- BLX-7006-CLN-001
- Status last verified
- Aug 2025
- First submitted
- 4 Aug 2025
- Last updated
- 24 Aug 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No