Status:
RECRUITING
A Two-Part First-In-Human Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GUB014295
Lead Sponsor:
AbbVie
Collaborating Sponsors:
Quotient Sciences
Conditions:
Healthy Volunteers
Overweight
Eligibility:
All Genders
18-65 years
Phase:
PHASE1
Brief Summary
This is a two-part, single centre, double-blind (within cohorts), randomised, placebo-controlled, single (Part 1) and multiple (Part 2) ascending subcutaneous dose study in lean to overweight or obese...
Detailed Description
This is a phase 1 clinical trial of a new long-acting amylin analogue GUB014295 in two parts. Trial design: Part 1 is a double-blind (within cohorts), randomised, placebo-controlled, single ascending...
Eligibility Criteria
Inclusion
- Males (Part 1 only) aged 18 to 55 years, and males and females (Part 2 only) aged 18 to 65 years inclusive at the time of signing informed consent
- Must agree to adhere to the contraception requirements
- Lean to overweight or obese but otherwise healthy males (Part 1 and 2) or nonpregnant, non-lactating females (Part 2 only)
- BMI of 22.0 to 32.0 kg/m2 for Part 1 and Part 2A, and a BMI of 27.0 to 35.0 kg/m2 for Part 2B and Part 2C, as measured at screening. Overweight or obese as assessed by BMI should be due to excess adipose tissue, as judged by the investigator
- Weight for males ≥70 kg (all parts), and for females ≥60 kg (Part 2 only) at screening
Exclusion
- Serious adverse reaction or serious hypersensitivity to any drug or formulation excipients
- Presence or history of clinically significant allergy requiring treatment, as judged by the investigator. Hay fever is allowed unless it is active
- Known or suspected hypersensitivity or allergy to paracetamol
- Presence or history of clinically significant cardiovascular, renal, hepatic, dermatological, respiratory, neurological, psychiatric, malignant, metabolic, endocrinological, haematological or venereal disorder, as judged by the investigator
- Presence or history of any clinically relevant gastrointestinal diseases or symptoms of gastrointestinal disorders potentially affecting interpretation of study data.
- Presence or history of diseases associated with impaired calcium homeostasis and/or increased bone turnover (e.g. Paget´s disease, osteoporosis)
- History of major depressive disorder within 2 years prior to screening
- Subjects unable to take paracetamol for any reason
- Subjects who do not have suitable veins for multiple venepunctures/cannulation as assessed by the investigator or delegate at screening
- Subjects with tattoos or scars on the abdomen which may interfere with injection site assessments as determined by the investigator or delegate at screening
- Clinically significant abnormal clinical chemistry, haematology, coagulation or urinalysis as judged by the investigator. Subjects with Gilbert's Syndrome are not allowed.
- HbA1c ≥48 mmol/mol (≥6.5%) and/or fasting plasma glucose ≥7.0 mmol/L at screening
- Part 2B only: Subjects with haemoglobin \<LLN at screening and/or admission
- Prolongation of the QTcF over 450 msec for males and 470 msec for females or any other clinically significant abnormal ECG results as judged by the investigator
- Supine blood pressure (after ≥5 min rest) \<90 mmHg or \>150 mmHg (systolic) and/or \<50 mmHg or \>90 mmHg (diastolic)
- Heart rate (ECG-recorded after ≥5 min rest) \<45 or \>90 beats per minute
- Positive hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV Ab) or human immunodeficiency virus (HIV) 1 and 2 antibody results
- Evidence of renal impairment at screening, as indicated by an estimated glomerular filtration rate (eGFR) of \<70 mL/min/1.73m2
- Part 2 only: Females who are pregnant or lactating (all female subjects must have a negative highly sensitive urine or serum pregnancy test)
- Subjects who have received any investigational medicinal product (IMP) in a clinical research study within the 90 days prior to Day 1, or less than 5 elimination half-lives prior to Day 1, whichever is longer
- Subjects who have previously been administered IMP in this study
- Donation of blood or plasma within the previous 3 months or loss of greater than 400 mL of blood
- Subjects who are taking, or have taken, any prescribed or over-the-counter drug or herbal remedies/vitamins in the 14 days before IMP administration.
- Paracetamol (up to 4 g per day) will be permitted except in the 48 h prior to the mixed meal tests on Day -1 and Day 4 (Part 1 Cohorts 2 to 6), Day 39 (Part 2A) and Day 81 (Part 2B) where paracetamol is not permitted.
- NSAIDs can be given at the discretion of the investigator to treat any AEs if necessary;
- Subject reports prior receipt of an amylin and/or calcitonin receptor agonist within the last 6 months
- History of any drug or alcohol abuse in the past 2 years
- Regular alcohol consumption \>21 units per week and in females \>14 units per week
- A confirmed positive alcohol breath test at screening or admission
- Current smokers and those who have smoked within the last 12 months
- Current users of e-cigarettes and nicotine replacement products and those who have used these products within the last 12 months
- A confirmed breath carbon monoxide reading of greater than 10 ppm at screening or admission
- Confirmed positive drugs of abuse test result at screening or admission
- Anticipated change in lifestyle (such as eating, exercise or sleeping pattern) during the trial and/or clinically significant body weight change (≥5% self-reported change) or comprehensive dieting attempts (e.g. participation in a weight reduction program or treatment with any medication indicated for weight management) within the last 90 days prior to screening
- Subjects who do not agree to consume the liquid mixed meal
- Male subjects with pregnant or lactating partners
- Any disorder, unwillingness or inability, not covered by any of the other exclusion criteria, that the investigator evaluates might jeopardise the subject's safety or compliance with the protocol
Key Trial Info
Start Date :
November 29 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2026
Estimated Enrollment :
124 Patients enrolled
Trial Details
Trial ID
NCT06144684
Start Date
November 29 2023
End Date
April 1 2026
Last Update
September 19 2025
Active Locations (1)
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1
Quotient Sciences
Nottingham, United Kingdom, NG11 6JS