An Open Label Study That Will Test Safety and Efficacy of RZL-012 Injection Into the Submental Fat in 10 Chinese vs. 10 Non-Chinese Subjects.
Study Details
Study Description
Brief Summary
This is a Phase 2, open label study that will consist of a screening period, baseline period in which subjects will receive a single treatment session and a follow-up period. The single treatment session will consist of multiple injections of RZL-012 into the submental area under the chin. Blood samples will be collected from all subjects for PK analyses in the first 30 hours after dosing. Subjects will thereafter be monitored for safety and efficacy for at least 84 days.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 1/Phase 2 |
Detailed Description
• RZL-012 (concentration of injected solution 50 mg/mL RZL-012) of 7.5 mg/0.15 mL/injection point that results in a total dose/volume of 240±30mg mg/4.8±0.6 mL RZL-012
Subjects treated with RZL-012 will undergo a single treatment session with 32±4 injections. The maximal number of injections will be 36 with maximal dose of 270 mg RZL-012 .
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: RZL-012 50mg/ml small synthetic molecule for submental fat reduction |
Drug: RZL-012
concentration of injected formulation 50 mg/mL RZL-012 of 7.5 mg/0.15 mL/injection point that results in a maximum total dose/volume of 240±30 mg/4.8±0.6 mL RZL-012
|
Outcome Measures
Primary Outcome Measures
- Pharmacokinetics measure - drug concentration in the blood (ng/mL) [48 hours]
Measurement of maximum drug concentration (Cmax) (ng/mL)
- Pharmacokinetics measure - Area under the plasma concentration versus time curve (AUC) (mg*h/L) [48 hours]
Secondary Outcome Measures
- Efficacy -Change in score according to Clinician chin assessment tool (C-CAT) [84 days]
To determine the efficacy of RZL-012 versus placebo on submental fat (SMF) reduction measured on Day 84 versus baseline using the Clinician Chin Assessment Tool (C-CAT). The CAT is composed of 5 points where 0 represents no fat and 4 represent very noticeable bulge and fat that extends beyond the neck
- Efficacy - Change in score according to Subject chin assessment tool (S-CAT) [84 days]
To determine the efficacy of RZL-012 versus placebo on submental fat (SMF) reduction measured on Day 84 versus baseline using the Subject Chin Assessment Tool (S-CAT). The CAT is composed of 5 points where 0 represents no fat and 4 represent very noticeable bulge and fat that extends beyond the neck
- Efficacy - Reduction in submental fat thickness [84 days]
Reduction from baseline in submental fatthickness (mm), as measured with MRI in RZL-012 treated subjects vs. placebo treated subjects on Day 84 following injection
- Safety - Adverse events follow up [84 days]
To evaluate the safety of RZL-012 subcutaneous injections in the submental area in Chinese vs. non Chinese population, as assessed by spontaneous adverse event reports and post injection evaluation of treatment area. Treatment area evaluations including, but not limited to evaluation of edema, bruising, dysphasia, dysphonia, erythema, dyspigmentation, induration, numbness, pain, paresthesia, and pruritus. The number of subjects with treatment-related adverse events will be compared within each treatment group, as assessed by CTCAE v4.0
Eligibility Criteria
Criteria
Inclusion Criteria:
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Is a male or female subject between the ages of 18 and 65 years, inclusive.
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Has body mass index (BMI) between >22 kg/m2 and <40 kg/m2.
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If enrolled for Chinese arm, subjects have to be ethnically pure, i.e., Chinese passport holders with all four grandparents being Chinese.
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Has a SMF bulge that is contiguous and fits to 32±4 injections sites according to a grid with 1 centimeter (cm) distance between injection points.
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Has grade 3 to 4 of SMF as rated by both the C-CAT and S-CAT.
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Has a visible or large pocket of submental fat- according to physician global assessment.
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Has stable weight, with no fluctuation of >5 kg in the past 12 months.
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If female, is not pregnant or breastfeeding based on the following:
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agree to the use of highly effective contraceptive methods for at least 2 weeks before baseline until 4 weeks after the last day of study drug and a negative serum pregnancy test (ß-hCG) at screening and negative urine pregnancy test at baseline; or
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is of nonchildbearing potential defined as clinically infertile as the result of surgical sterilization (hysterectomy, bilateral tubal ligation, and/or bilateral oophorectomy); or
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is confirmed postmenopausal status (defined as either having amenorrhea for ≥ 12 consecutive months without another cause and documented serum follicle-stimulating hormone (FSH) level > 40 mIU/mL or another documented medical condition (e.g., was born without a uterus))
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If male (with or without vasectomy), agree to the use of highly effective contraceptive methods as listed above in criteria 7 as well as to use a barrier method, e.g. condom , from study check-in until 7 days after the last day of study drug.
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Is willing to avoid strenuous exercise for seven (7) days post treatment.
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Is able to adhere to the visit schedule and protocol requirements and be available to complete the study.
- Is willing and able to sign an Institutional Review Board (IRB) approved informed consent form (ICF) indicating that they are aware of the investigational nature of the study.
Exclusion Criteria:
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Is unable to tolerate subcutaneous injections.
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Has dysfunctional gallbladder activity (e.g., underwent cholecystectomy or cholecystitis).
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Has any uncontrolled systemic disease that is not stabilized (i.e., cardiovascular disease, mental illness).
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Has skin laxity (i.e., elastosis, skin crepiness, skin redundancy, skin draping, vertical and/or horizontal skin bands and folds, blunting of cervical mental angle, loss of opposition of skin to underlying neck structures due to skin laxity) that could obscure the evaluation and treatment of SMF.
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Has any scars, unshaven hair, tattoos, facial hair or jewelry on or near the proposed treatment area.
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Has presence of structures or confounding factors that may interfere with assessing SMF such as but not limited to enlarged submandibular salivary and/or parotid glands, micrognanthia, chin implant, soft tissue volume augmentation of chin and/or jawline, pronounced platysmal bands and deep necklace lines or presence of facial jowls that could obscure the evaluation of SMF.
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Has a fat bulge under the chin that is too large to be adequately treated by 32±4 contiguous injections on a 1cm grid .
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Has a fat bulge under the chin that is of an insufficient volume to allow 32±4 injections within a contiguous 1 cm grid.
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Has significant history or current evidence of a medical, psychological or other disorder that, in the Investigator's opinion, would preclude enrollment in the study.
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Has an active bacterial, fungal, or viral infection in the proposed treatment area.
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Has a pre-existing skin condition in the submental region that, at the Investigator's discretion, may confound evaluation or analysis.
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Has previously had treatments or surgery in the submentum, such as but not limited to, focused ultrasound, radiofrequency, cryolipolysis, liposuction, sodium deoxycholate, or neck lift.
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Has pre-existing neurological or gastrointestinal condition leading to dysphagia, dysphonia, or facial nerve palsy.
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Has Dercum's Disease.
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Has allergic reactions to injectables.
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Has any pre-existing medical condition other than increased SMF that, at the Investigator's discretion, may result in increased submental fullness, such as but not limited to, thyroid enlargement, goiter, cervical lymphadenopathy, etc.
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Has a planned fat reduction procedure of any variety to the submental region for the duration of the study.
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Has medication or a history of coagulopathy.
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Has a history or family history of venous thrombotic disease.
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Has been treated chronically at least three (3) months prior to study entry with systemic steroids or immunosuppressive drugs.
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Has been treated chronically at least one (1) week prior to study entry with non-steroidal anti-inflammatory drugs (NSAIDs)
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Has used anticoagulation therapies that may increase bleeding or bruising (i.e., aspirin, ibuprofen, warfarin, vitamins, and herbal preparations) for seven (7) days prior to treatment.
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Has had treatment with botulinum toxin injections in the neck or chin area within 9 months prior to screening.
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Current participation or participation within three (3) months prior to the start of this study in a drug or other investigational research study.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Raziel Therapeutics Ltd.
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- RZL-012-SMFC-P2US-001