Study to Assess PK, Safety and Tolerability in Patients With DM and CKD

Diabetes Clinical Trial

Official title:

A Multi-Center Open-label Investigation to Assess the Pharmacokinetics, Safety and Tolerability of DM199 in Patients With Diabetes Mellitus and Chronic Kidney Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03795389
• Other study ID #: DM199-2018-001
• Status: Completed
• Phase: Phase 1
• Start date: February 12, 2019
• Est. completion date: July 21, 2019

Study information

• Verified date: July 2019
• Source: DiaMedica Therapeutics Inc
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

An open-label, phase IB, multi-center study evaluating DM199 in subjects with Type 1 Diabetes or Type 2 Diabetes and Stage 3 or 4 Chronic Kidney Disease. The primary objectives of this study are to evaluate safety, tolerability, and PK profile of DM199 in these subjects.

Description:

The study evaluates the safety, tolerability, and PK profile of DM199 in subjects with T1D or T2D and with Stage 3 or Stage 4 CKD. Additionally, this study evaluates urine concentrations of KLK1 pre and post dose. Cohort 1: Subjects with T1D or T2D and Stage 3 CKD will be administered one of three DM199 doses: 3.0 ug/kg or 5.0 ug/kg or 8.0 ug/kg single SC dose. Cohort 2: Subjects with T1D or T2D and Stage 4 CKD will be administered a single 3.0 µg/kg single SC dose. Secondary and exploratory study objectives include collection and analysis of vital signs, biomarkers, eGFR, blood glucose, and ECG's.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 33
• Est. completion date: July 21, 2019
• Est. primary completion date: July 21, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Subject is willing and able to provide informed consent for study participation.
• Subject is = 18 years of age.
• Subject has an established diagnosis of T1D or T2D as determined by medical evaluation at screen.
• Subjects A1c <9.8%
• Subject is clinically stable with respect to underlying renal impairment and diabetes, as assessed by the Investigator's medical evaluation.
• Subject has been diagnosed with Stage 3 CKD as defined by eGFR (MDRD) between 30 - <60 or Stage 4 as defined by eGFR <30 (not on dialysis) at screening.
• Subject has a body mass index (BMI) between 18 to 45 kg/m2 (inclusive).

Exclusion Criteria:

• Subject has positive drug test for drugs of abuse and/or positive alcohol breath test at screening and Day 0.
• Subject is unable or unwilling to comply with protocol requirements, including assessments, tests, and follow-up visits.
• Subject has a history of significant allergic diathesis such as urticaria, angioedema, or anaphylaxis.
• Subject has had any live vaccination = 3 months prior to enrollment or will require vaccination during the study.
• Subject must not be taking an ACEi medication for 5 half-lives prior to study drug administration and for 5 days post study drug administration.
• Subject is unwilling or unable to limit smoking to = 10 cigarettes per day (or other products that contain nicotine limited to < 200 mg of nicotine/day) during the study participation period.
• Subject has a current malignancy or active malignancy = 3 years prior to enrollment except basal cell or squamous cell carcinoma of the skin or in situ cervical cancer that has undergone potentially curative therapy and = six months have elapsed since the procedure.
• Subject has an active infection at the time of enrollment, and/or a history of clinically significant acute bacterial, viral, or fungal systemic infections that required systemic treatment in the last four weeks prior to enrollment.
• Subject has known medical history of alpha 1-antitrypsin deficiency (a1-antitrypsin deficiency).
• Subject has serological evidence of human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or anti-hepatitis C virus (Anti-HCV) at screen.
• Subject is pregnant or nursing or is planning a pregnancy during the study period.
• Subject is male or female of childbearing potential, is participating in sexual activity that could lead to pregnancy and is unable or unwilling to practice medically effective contraception during the study.
• Subject has received any investigational drug or device within 14 days (or 5 half lives, whichever is longer) prior to study drug administration on Day 1
• Subject has renal artery stenosis as determine at screen with medical history.
• Subject has hypotension as defined by systolic blood pressure = 90 and diastolic blood pressure = 60 mmHg.
• Subject has Proteinuria: PCR>2000mg/gm (spot testing).
• Subject does not have adequate venous access for blood sampling.
• Subject has any other medical condition which, in the opinion of the Investigator, will make participation medically unsafe or interfere with the study results.
• Subject has any other clinically significant abnormalities in laboratory test results at screening that would, in the opinion of the Investigator, increase the subject's risk of participation, jeopardize complete participation in the study, or compromise interpretation of study data.
• Subject has any of the following conditions as determined by ECG or medical record:
• Any significant arrhythmia or conduction abnormality, which, in the opinion of the Investigators and Medical Monitor, may interfere with the safety of the subject.
• Subject is taking Cimetidine, St. John's Wort, or any other herbal or probiotic supplement.

Related Conditions & MeSH terms

• Chronic Kidney Disease
• Chronic Kidney Disease, Stage 3 (Moderate)
• Chronic Kidney Disease, Stage 4 (Severe)
• Diabetes
• Kidney Diseases
• Renal Insufficiency, Chronic

Intervention

Drug:
• DM199
Single SC dose

Locations

Country	Name	City	State
United States	Clinical Pharmacology of Miami	Hialeah	Florida
United States	Orlando Clinical Research Center Inc	Orlando	Florida
United States	Prism Research	Saint Paul	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
DiaMedica Therapeutics Inc

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	serum creatinine		11 days
Other	Blood glucose		11 days
Primary	Safety as assessed by incidence, severity, and causality of adverse events		11 days
Primary	Tolerability as assessed by incidence and severity of AEs		11 days
Primary	plasma measurements of DM199	as measured in the three different dosing groups; 3.0 ug/kg, 5.0 ug/kg, and 8.0 ug/kg.	11 days
Primary	DM199 urine concentrations of KLK1	urine KLK1 will be measured pre and post study drug administration.	11 days
Secondary	C Reactive protein (CRP)		11 days
Secondary	Matrix Metalloproteinase-9 (MMP-9)		11 days
Secondary	Vascular Endothelial Growth Factor (VEGF)		11 days
Secondary	Nitric Oxide (NO)		11 days
Secondary	Serum creatinine		11 days
Secondary	Cystatin C		11 days
Secondary	neutrophil gelatinase-associated prostaglandin E2		11 days
Secondary	Urine Kidney Injury Molecule-1 (Kim1)		11 days