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Multiple Ascending Dose Study of GMC-252-L-Lys Salt in Healthy Subjects and Type 2 Diabetics

11. oktober 2017 opdateret af: Genmedica Therapeutics S.L.

A Double Blind, Placebo-controlled, Randomised, Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of GMC-252 in Healthy Male Subjects and Male Type 2 Diabetics

The purpose of this study is to assess the safety, tolerability and pharmacokinetics (PK) of multiple oral doses of GMC-252-L-Lysine salt (GMC-252) in healthy subjects and type 2 diabetics.

The secondary objective is to explore the effect of multiple oral doses of GMC-252 on pharmacodynamic(PD) parameters in type 2 diabetics.

Studieoversigt

Status

Afsluttet

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

34

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Belfast, Det Forenede Kongerige, BT2 7BA
        • BioKinetic Europe Ltd.
      • Merthyr Tydfil, Det Forenede Kongerige, CF48 4DR
        • Simbec Research Ltd

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 55 år (Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Han

Beskrivelse

Inclusion Criteria

Part 1 (Healthy Subjects) and Part 2 (Type 2 Diabetic Patients):

  1. Diet: Able to eat standard food, no vegetarians.
  2. Compliance: Understands and is willing, able and likely to comply with all study procedures and restrictions.
  3. Consent: Demonstrates understanding of the study and has given signed, voluntary written informed consent.
  4. Have no known hypersensitivity to diflunisal, NAC or other NSAIDs.
  5. No history of blood diseases including but not limited to clinically significant platelet diseases and coagulation abnormalities.
  6. No clinically relevant gastrointestinal disease.
  7. Have an estimated creatinine (CREA) clearance>70 mL/min/surface area (CREA clearance will be calculated from the serum CREA value by using the Cockroft and Gault formula).
  8. Have no history of heart failure or uncontrolled hypertension or other known clinically significant cardiovascular disease.
  9. Have no history of bronchial asthma or 'Aspirin Triad' (chronic rhino-sinusitis with polyps, severe asthma and intolerance to aspirin or other NSAIDs).
  10. Have no clinically significant abnormality of liver tests before entry into the study.
  11. A negative urinary drugs of abuse screen, determined within 28 days before the first dose (N.B. a positive alcohol result may be repeated at the discretion of the Investigator).
  12. Negative human immunodeficiency virus (HIV) and hepatitis B surface antigen (Hep B) and hepatitis C virus antibody (Hep C) results.
  13. No clinically significant abnormalities in a 12-lead ECG determined within 28 days before the first dose.
  14. No history of clinically significant renal disease or any food intolerance.
  15. Willing to use 2 effective methods of contraception i.e. established method of contraception + condom, if applicable (unless anatomically sterile or where abstaining from sexual intercourse is in line with the preferred and usual lifestyle of the subject) from Day 1 until 3 months afterwards.

Additional Criteria for Part 1 (Healthy Subjects):

  1. Healthy males aged 18 to 55 inclusive.
  2. Body mass index (BMI) within the range of 18-30 kg/m2 inclusive.
  3. Non-Smokers (including e-cigarettes) who have abstained from smoking for at least 6 months.

Additional Criteria for Part 2 (Type 2 Diabetic Patients):

  1. Males aged 18 to 65 inclusive. BMI within the range of 18-38 kg/m2 inclusive.
  2. Diagnosis of T2DM according to the World Health Organization criteria.
  3. HbA1c between 7.0% and 12.0 % inclusive.
  4. Currently treated with metformin with a stable treatment regimen for 3 months or more prior to the Screening Visit, and not receiving other anti-diabetic medications. Allowed medication during the study include metformin, statin (3-hydroxy-3-methylglutaryl-coenzyme A (HMG CoA) reductase inhibitors), paracetamol up to 3 g/day, low doses of aspirin and antihypertensive drugs if the doses are not changed in the 3 months before the start of screening. Other allowed medications will be approved by PI and Sponsor before a patient can be enrolled. Diflunisal (a test drug component) may decrease the antihypertensive activityof many of the currently used antihypertensive medications, such as β-blockers, alpha (α)-blockers, loop diuretics, angiotensin converting enzyme (ACE inhibitors), angiotensin 2 receptor blockers, calcium channel blockers. Therefore, patients who are on current stable antihypertensive medications will be subjected to close monitoring of their blood pressure throughout the study.
  5. Stable dietary habits and regimen of treatment for concomitant diseases for 1 month or more prior to the Screening Visit.
  6. Subject able and willing to undergo oral glucose tolerance test (OGTT).

Exclusion Criteria

Part 1 (Healthy Subjects) and Part 2 (Type 2 Diabetic Patients):

  1. A clinically significant history of previous allergy / sensitivity to any of the GMC-252 components, NAC or diflunisal.
  2. Inability to communicate well with the Investigator (i.e., language problem, poor mental development or impaired cerebral function).
  3. Participation in a New Chemical Entity clinical study within the previous 4 months or a marketed drug clinical study within the previous 3 months. (N.B. washout period between studies is defined as the period of time elapsed between the last dose of the previous study and the first dose of the next study).
  4. Donation of 450 mL or more blood within the previous 3 months.
  5. A clinically significant history of drug, alcohol or other substance abuse in the past 2 years.

Additional Criteria for Part 1 (Healthy Subjects):

  1. A clinically significant history of gastrointestinal disorder likely to influence drug absorption.
  2. Receipt of regular medication within 28days of the first dose that may have an impact on the safety and objectives of the study (at the Investigator's discretion).
  3. Evidence of renal, hepatic, central nervous system, respiratory, cardiovascular or metabolic dysfunction.

Additional Criteria for Part 2 (Type 2 Diabetic Patients):

  1. Diagnosis/General Health:

    • Diabetic autonomic or sensory neuropathy including gastroparesis, diabetic nephropathy or untreated active proliferative retinopathy.
    • Clinically significant abnormalities in laboratory evaluation (including clinical biochemistry, haematology and urinalysis) in the opinion of the Investigator.
  2. Diseases:

    • Uncontrolled hypertension (blood pressure ≥ 160/100 mmHg), severe or unstable angina, coronary insufficiency, congestive heart failure, clinically significant (in the opinion of the Investigator) renal or hepatic disease.
    • Previous gastric or intestinal surgerythat might impact drug absorption.
    • Malignancy within 5 years of the start of the study, except for successfully treated local basal cell carcinoma
    • Current or relevant previous history, of clinically significant psychiatric illness.
  3. Medications:

    • Current use of insulin or any previous use of insulin other than as part of a clinical trial or associated with surgical procedure or acute illness for up to 7 days.
    • Use of any anti diabetic medication other than metformin in the 3 months prior to study entry.
    • Current use of any anticoagulant drug e.g. warfarin, heparin.
    • Prior use (within 48 h of dosing) of any drug that could have altered gastric motility (domperidone, cyclizine, metoclopramide, prochlorperazine), or cholestyramine.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Cohort 1 (Part 1)

Multiple ascending oral administrations of GMC-252-L-Lysine Salt and matching placebo

Interventions:

Drug: GMC-252-L-Lysine Salt Other: Placebo

1 dose by oral route, once a day, 28 days
Andre navne:
  • GMC-252-L-Lys Salt
Matching doses by oral route, once a day, 28 days
Placebo komparator: Cohort 2 (Part 1)

Multiple ascending oral administrations of GMC-252-L-Lysine Salt and matching placebo

Interventions:

Drug: GMC-252-L-Lysine Salt Other: Placebo

1 dose by oral route, once a day, 28 days
Andre navne:
  • GMC-252-L-Lys Salt
Matching doses by oral route, once a day, 28 days
Placebo komparator: Cohort 3 (Part 1)

Multiple ascending oral administrations of GMC-252-L-Lysine Salt and matching placebo

Interventions:

Drug: GMC-252-L-Lysine Salt Other: Placebo

1 dose by oral route, once a day, 28 days
Andre navne:
  • GMC-252-L-Lys Salt
Matching doses by oral route, once a day, 28 days
Placebo komparator: Cohort 4 (Part 2)

Multiple ascending oral administrations of GMC-252-L-Lysine Salt and matching placebo

Interventions:

Drug: GMC-252-L-Lysine Salt Other: Placebo

1 dose by oral route, once a day, 28 days
Andre navne:
  • GMC-252-L-Lys Salt
Matching doses by oral route, once a day, 28 days

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Number of Participants with Serious and Non-Serious Adverse Events
Tidsramme: 28 days plus 14 days post last dose
Physical status (Vital signs; 12-lead ECG; Urinalysis; Haematology and biochemistry)
28 days plus 14 days post last dose

Sekundære resultatmål

Resultatmål
Tidsramme
Maximal Concentration (Cmax)
Tidsramme: 28 days plus 14 days post last dose
28 days plus 14 days post last dose
Area Under the Concentration-Time Curve
Tidsramme: 28 days plus 14 days post last dose
28 days plus 14 days post last dose
Time to reach steady state
Tidsramme: 28 days plus 14 days post last dose
28 days plus 14 days post last dose

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Preliminary effect on Fasting blood glucose (Cohort 4 only)
Tidsramme: 28 days plus 14 days post last dose
28 days plus 14 days post last dose
Preliminary effect on oral glucose tolerance test (OGTT) (Cohort 4 only)
Tidsramme: 28 days plus 14 days post last dose
28 days plus 14 days post last dose
Preliminary effect on Insulin levels (Cohort 4 only)
Tidsramme: 28 days plus 14 days post last dose
Insulin
28 days plus 14 days post last dose
Preliminary effect on C-Peptide levels (Cohort 4 only)
Tidsramme: 28 days plus 14 days post last dose
28 days plus 14 days post last dose
Preliminary effect on Fructosamine levels (Cohort 4 only)
Tidsramme: 28 days plus 14 days post last dose
28 days plus 14 days post last dose
Preliminary effect on %HbA1c (Cohort 4 only)
Tidsramme: 28 days plus 14 days post last dose
28 days plus 14 days post last dose

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Samarbejdspartnere

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. april 2016

Primær færdiggørelse (Faktiske)

1. september 2017

Studieafslutning (Faktiske)

1. september 2017

Datoer for studieregistrering

Først indsendt

13. april 2016

Først indsendt, der opfyldte QC-kriterier

15. april 2016

Først opslået (Skøn)

20. april 2016

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

12. oktober 2017

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

11. oktober 2017

Sidst verificeret

1. oktober 2017

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • GMC-252-1.03

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

Uafklaret

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med GMC-252-L-Lysine Salt

Abonner