Single Ascending Dose Study With Healthy Male Volunteers and Type II Diabetic Patients
NCT00886366 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 26
Last updated 2010-12-07
Summary
The purpose of this study is to assess safety and tolerability of AZD6714 after single ascending oral doses in healthy male subjects and type 2 diabetic patients.
Conditions
Interventions
- DRUG
-
AZD6714
Oral single doses a-h suspension
- DRUG
-
Oral single doses suspension
- DRUG
-
AZD6714
Oral single doses a-d suspension
- DRUG
-
AZD6714
Oral single doses d and g suspension
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Klas Malmberg, MD, PhD · AstraZeneca R&D Mölndal
-
Marianne Hartford · CPU Sahlgrenska University Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 20 Years
- Max Age
- 40 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2009-04-30
- Primary Completion
- 2009-09-30
- Completion
- 2009-09-30
Countries
- Sweden
Study Locations
More Related Trials
-
Assessment of the Safety, Tolerability and Pharmacodynamics After Administration of One Dose of AZD8601 to Male Patients With Type II Diabetes Mellitus (T2DM)
NCT02935712 ·Status: COMPLETED ·Phase: PHASE1
-
To Evaluate Safety and Tolerability After Multiple Oral Doses of AZD1656 in Type 2 Diabetes Patients on Top of Insulin
NCT00768105 ·Status: COMPLETED ·Phase: PHASE1
-
To Study Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AZD1656 in Japanese Type 2 Diabetes Mellitus (T2DM) Patients
NCT00916604 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Investigate Multiple Ascending Doses of AZD5004 in Healthy Japanese Participants and Participants With Type 2 Diabetes Mellitus
NCT06703658 ·Status: COMPLETED ·Phase: PHASE1
-
Japan Dose Regimen Study of AZD1656 in Japanese Type 2 Diabetes Mellitus Patients
NCT01152385 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate P-Glucose, Safety and Tolerability After Oral Single Dosing of AZD6370 in Type 2 Diabetic Patients
NCT00690287 ·Status: COMPLETED ·Phase: PHASE1
-
To Evaluate Safety and Tolerability After Multiple Oral Doses of AZD1656 in Type 2 Diabetes Patients on Top of Metformin
NCT00774553 ·Status: COMPLETED ·Phase: PHASE1
-
To Assess Safety, Tolerability, Pharmacokinetics/Pharmacodynamics and the Effect of Fasting After Single Oral Doses of AZD5658 in Type 2 Diabetes
NCT01176097 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Assess the Safety and Tolerability After Multiple Oral Doses of AZD1656 in Patients With Type 2 Diabetes Mellitus Treated With Metformin
NCT00817778 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Investigate in Healthy Volunteers (Part 1) and in Patients With Type 2 Diabetes Mellitus (Part 2) the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Doses of RO6799477
NCT02164266 ·Status: COMPLETED ·Phase: PHASE1
-
A Multiple Ascending Dose Phase I Study of DBPR108 in Healthy Male Subjects
NCT02163278 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Assess the Absorption, Distribution, Metabolism and Excretion of AZD1656 in Type 2 Diabetes Mellitus (T2DM)
NCT00960791 ·Status: COMPLETED ·Phase: PHASE1
-
Single Ascending Dose Trial in Patients With Type 2 Diabetes
NCT01492465 ·Status: TERMINATED ·Phase: PHASE1
-
Study to Assess the Effect on Glucose Homeostasis of Two Dose Levels of AZD9567, Compared to Prednisolone, in Adults With Type 2 Diabetes
NCT04556760 ·Status: COMPLETED ·Phase: PHASE2
-
Study to Assess Safety, Tolerability, PK, and PD of Multiple Doses of ZE63-0302 Administrated Orally in T2DM Patients.
NCT07234864 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1
-
Study to Evaluate the Analgesic Efficacy of 28 Days' Oral Administration of AZD2066 Compared With Placebo in Patients With Painful Diabetic Neuropathy
NCT00857623 ·Status: COMPLETED ·Phase: PHASE2
-
A Phase I Study to Assess the Pharmacodynamics of Oral AR-C165395XX in Subjects With Type 2 Diabetes Mellitus (T2DM)
NCT02367066 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Tolerability of AZD1656 in Type 2 Diabetes Mellitus (T2DM) Patients Treated With Metformin and Sulfonylurea
NCT00995787 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Tolerability of Ascending Intravenous Doses of PF-05231023 In Adult Subjects With Type 2 Diabetes
NCT01396187 ·Status: COMPLETED ·Phase: PHASE1
-
Clinical Study to Assess the Pharmacokinetics, Safety and Tolerability of SRT2104 Administered to Normal Healthy Male Volunteers
NCT00933062 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy, Safety, and Tolerability of Once Daily Oral Administration of AZD5004 Versus Placebo for 26 Weeks in Adults With Type 2 Diabetes Mellitus.
NCT06579105 ·Status: COMPLETED ·Phase: PHASE2
-
Multiple Ascending Dose Study in Subjects With Type 2 Diabetes
NCT01856881 ·Status: TERMINATED ·Phase: PHASE1
-
Efficacy and Safety of Exenatide in Japanese Patients With Type 2 Diabetes Who Are Treated With Oral Antidiabetic(s)
NCT00577824 ·Status: COMPLETED ·Phase: PHASE3
-
A Study Of PF-05190457 In Healthy Volunteers And Type-2 Diabetic Patients
NCT01372163 ·Status: TERMINATED ·Phase: PHASE1
-
Single Ascending Oral Doses of SY-009 in Healthy Subjects
NCT04119947 ·Status: COMPLETED ·Phase: PHASE1