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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00850239
Other study ID # PHX1149-PROT302
Secondary ID
Status Terminated
Phase Phase 3
First received February 20, 2009
Last updated August 10, 2010
Start date May 2009
Est. completion date December 2010

Study information

Verified date August 2010
Source Phenomix
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug AdministrationUnited States: Institutional Review BoardCzech Republic: State Institute for Drug ControlCzech Republic: Ethics CommitteeRomania: Ministry of Public HealthRomania: National Medicines AgencyPoland: Ministry of Healthnd: Office for Registration of Medicinal Products, Medical Devices and Biocidal ProductsIndia: Drugs Controller General of IndiaPeru: Ethics CommitteePeru: Ministry of HealthArgentina: Administracion Nacional de Medicamentos, Alimentos y Tecnologia MedicaArgentina: Human Research Bioethics CommitteeChile: Instituto de Salud Pública de ChileChina: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to demonstrate the efficacy of dutogliptin over 26 weeks (as evidenced by placebo-corrected changes in HbA1c relative to baseline), to demonstrate safety and tolerability of dutogliptin, and to demonstrate changes in fasting plasma glucose over 26 weeks.


Recruitment information / eligibility

Status Terminated
Enrollment 700
Est. completion date December 2010
Est. primary completion date October 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Type 2 diabetes mellitus, diagnosed at least 4 months prior to Screening (Visit 1)

- Age 18 to 85 years, inclusive.

- Male and non-pregnant, non-lactating (and not planning to become pregnant during the study) female subjects with a BMI of 20 to 48 kg/m2, inclusive

- Current treatment of Type 2 diabetes mellitus with a stable dose of metformin of = 2000 mg (or the highest tolerated dose) used in accordance with product labeling for at least 6 weeks prior to screening (Visit 1)

- HbA1c 7.0% - 10.0%, inclusive; and fasting plasma C peptide greater than 0.26 nmol/L (> 0.8 ng/mL; > 281 pmol/L) at screening (Visit 1)

Exclusion Criteria:

- Type 1 diabetes mellitus

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Drug:
dutogliptin
400 mg
placebo


Locations

Country Name City State
Argentina Phenomix Investigational Site 401 Buenos Aires
Argentina Phenomix Investigational Site 402 Buenos Aires
Argentina Phenomix Investigational Site 404 Buenos Aires
Argentina Phenomix Investigational Site 405 Buenos Aires
Argentina Phenomix Investigational Site 406 Buenos Aires
Argentina Phenomix Investigational Site 407 Buenos Aires
Argentina Phenomix Investigational Site 408 Buenos Aires
Argentina Phenomix Investigational Site 409 Buenos Aires
Argentina Phenomix Investigational Site 411 Buenos Aires
Argentina Phenomix Investigational Site 403 Corrientes
Argentina Phenomix Investigational Site 410 Mendoza
Argentina Phenomix Investigational Site 400 Rosario
Chile Phenomix Investigational Site 502 Santiago
Chile Phenomix Investigational Site 504 Santiago
Chile Phenomix Investigational Site 505 Santiago
Chile Phenomix Investigational Site 500 Temuco
Chile Phenomix Investigational Site 501 Temuco
Czech Republic Phenomix Investigational Site 209 Chodov
Czech Republic Phenomix Investigational Site 205 Havírov-Mesto
Czech Republic Phenomix Investigational Site 204 Liberec
Czech Republic Phenomix Investigational Site 202 Olomouc
Czech Republic Phenomix Investigational Site 206 Ostrava Kuncice
Czech Republic Phenomix Investigational Site 208 Praha
Czech Republic Phenomix Investigational Site 203 Prostejov
Czech Republic Phenomix Investigational Site 207 Unicov
Czech Republic Phenomix Investigational Site 201 Valašské Klobouky
India Phenomix Investigational Site 701 Bangalore Karnataka
India Phenomix Investigational Site 702 Bangalore Karnataka
India Phenomix Investigational Site 708 Chennai
India Phenomix Investigational Site 709 Gopalapuram Chennai
India Phenomix Investigational Site 703 Hyderabad Andhara Pradesh
India Phenomix Investigational Site 706 Indore Madhya Pradesh
India Phenomix Investigational Site 711 Mumbai Maharastra
India Phenomix Investigational Site 700 Nashik Maharashtra
India Phenomix Investigational Site 710 Navi Mumbai Maharashtra
India Phenomix Investigational Site 707 Shastrinagar Jaipur
India Phenomix Investigational Site 705 Trivandrum Kerala
India Phenomix Investigational Site 704 Visakhapatanam Andhra Pradesh
Peru Phenomix Investigational Site 607 Arequipa
Peru Phenomix Investigational Site 605 Cercado de Lima
Peru Phenomix Investigational Site 601 Ica
Peru Phenomix Investigational Site 600 Lima
Peru Phenomix Investigational Site 603 Lima
Peru Phenomix Investigational Site 604 Lima
Peru Phenomix Investigational Site 608 Lima
Peru Phenomix Investigational Site 610 Lima
Peru Phenomix Investigational Site 606 Piura
Peru Phenomix Investigational Site 602 Trujillo
Peru Phenomix Investigational Site 609 Wanchaq Cusco
Poland Phenomix Investigational Site 300 Gdansk
Poland Phenomix Investigational Site 301 Gdansk
Poland Phenomix Investigational Site 303 Katowice
Poland Phenomix Investigational Site 312 Katowice
Poland Phenomix Investigational Site 309 Kraków
Poland Phenomix Investigational Site 313 Kraków
Poland Phenomix Investigational Site 308 Lublin
Poland Phenomix Investigational Site 310 Poznan
Poland Phenomix Investigational Site 306 Pulawy
Poland Phenomix Investigational Site 304 Szczecin
Poland Phenomix Investigational Site 305 Warszawa
Poland Phenomix Investigational Site 307 Warszawa
Poland Phenomix Investigational Site 311 Warszawa
Poland Phenomix Investigational Site 302 Wroclaw
United States Phenomix Investigational Site 116 Albuquerque New Mexico
United States Phenomix Investigational Site 105 Anaheim California
United States Phenomix Investigational Site 138 Biloxi Mississippi
United States Phenomix Investigational Site 131 Brick New Jersey
United States Phenomix Investigational Site 136 Brockton Massachusetts
United States Phenomix Investigational Site 135 Chicago Illinois
United States Phenomix Investigational Site 123 Chico California
United States Phenomix Investigational Site 130 Cincinnati Ohio
United States Phenomix Investigational Site 143 Coral Gables Florida
United States Phenomix Investigational Site 118 Cuyahoga Falls Ohio
United States Phenomix Investigational Site 102 Dallas Texas
United States Phenomix Investigational Site 139 Dallas Texas
United States Phenomix Investigational Site 141 Dunwoody Georgia
United States Phenomix Investigational Site 126 El Paso Texas
United States Phenomix Investigational Site 134 Escondido California
United States Phenomix Investigational Site 112 Greenville South Carolina
United States Phenomix Investigational Site 142 Hialeah Florida
United States Phenomix Investigational Site 101 Honolulu Hawaii
United States Phenomix Investigational Site 124 Indianapolis Indiana
United States Phenomix Investigational Site 127 Indianapolis Indiana
United States Phenomix Investigational Site 119 Jacksonville Florida
United States Phenomix Investigational Site 125 Kalamazoo Michigan
United States Phenomix Investigational Site 100 Kenosha Wisconsin
United States Phenomix Investigational Site 133 Kissimmee Florida
United States Phenomix Investigational Site 122 Las Vegas Nevada
United States Phenomix Investigational Site 140 Las Vegas Nevada
United States Phenomix Investigational Site 103 Long Beach California
United States Phenomix Investigational Site 106 Los Angeles California
United States Phenomix Investigational Site 115 Montgomery Alabama
United States Phenomix Investigational Site 104 San Antonio Texas
United States Phenomix Investigational Site 121 Tempe Arizona
United States Phenomix Investigational Site 137 Tempe Arizona
United States Phenomix Investigational Site 110 Trenton New Jersey
United States Phenomix Investigational Site 107 Winston-Salem North Carolina

Sponsors (2)

Lead Sponsor Collaborator
Phenomix Forest Laboratories

Countries where clinical trial is conducted

United States,  Argentina,  Chile,  Czech Republic,  India,  Peru,  Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Primary objective is to demonstrate the efficacy of dutogliptin, as evidenced by placebo-corrected changes in HbA1c relative to baseline. 26 weeks No
Secondary Demonstrate safety and tolerability of dutogliptin 26 weeks Yes
Secondary • Demonstrate changes in fasting plasma glucose 26 weeks No
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