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A Phase 1 Study of DD01 in Overweight/Obese Subjects With T2DM and NAFLD

Primary Purpose

Overweight and Obesity, Type2 Diabetes, NAFLD

Status
Recruiting
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
DD01
Placebo
Sponsored by
Neuraly, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overweight and Obesity focused on measuring Liver Disease

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Part A Inclusion Criteria:

  • Type 2 diabetes ≥ 12 months.
  • Treatment with diet and exercise or metformin monotherapy on stable dose for 3 months prior to screening
  • HbA1c ≤ 10%).
  • Body Mass Index (BMI) ≥ 25 and ≤ 40.0 kg/m2

Part B Inclusion Criteria

  • Type 2 diabetes ≥ 12 months.
  • Treatment with diet and exercise or metformin monotherapy on stable dose for 3 months prior to screening
  • HbA1c ≤ 10%
  • BMI ≥ 30 kg/m2 and ≤ 40.0 kg/m2
  • Waist circumference ≤ 57 inches
  • Controlled attenuation parameter by FibroScan
  • Liver fat fraction ≥ 10% by magnetic resonance imaging (MRI)

Part A Exclusion Criteria:

  • History of type 1 diabetes mellitus (T1DM)
  • History of acute proliferative retinopathy or maculopathy, severe gastroparesis, and/or severe neuropathy, in particular autonomic neuropathy, as judged by the Investigator.
  • Uncontrolled hypertension
  • Treatment with antihypertensive medication and statins not stable during the past 2 months prior to screening
  • Treatment with thyroid hormones not stable during the past 3 months prior to screening
  • History of any weight control treatment, including over-the-counter and herbal medication and supplements, or any medication with a labeled indication for weight loss or weight gain within 3 months prior to screening
  • History of surgical treatment for obesity
  • History of heart disease
  • History of renal disease
  • History or current diagnosis of acute or chronic pancreatitis or factors for pancreatitis, such as a history of cholelithiasis (without cholecystectomy) or alcohol abuse
  • A history of or active chronic liver disease due to alcohol, auto-immune, HIV, HBV or active HCV-infection or NASH
  • History of major depression, anxiety, suicidal behavior or attempts, or other psychiatric disorder requiring medical treatment
  • Personal or family history of medullary thyroid carcinoma (MTC) or a genetic condition that predispose to MTC (i.e., multiple endocrine neoplasia type 2)
  • Administration of Vaccines/Immunizations within 14 days prior to first dosing or if scheduled during the study. Vaccination for COVID-19 is allowed during the study if a washout period of 5 days after vaccine administration is followed before dosing.
  • History of any major surgery within 6 months prior to screening
  • Participation in any other clinical interventional study receiving active treatment within 30 days or 5 half-lives prior to screening, whichever is longer
  • History of alcohol or illicit drug abuse including marijuana
  • Existence of any surgical or medical condition that, in the judgment of the Investigator, might interfere with the investigational product

PART B Exclusion Criteria

  • History of type 1 diabetes mellitus (T1DM)
  • History of acute proliferative retinopathy or maculopathy, severe gastroparesis, and/or severe neuropathy, in particular autonomic neuropathy, as judged by the Investigator
  • Uncontrolled hypertension (treatment with medications must be stable)
  • History of any weight control treatment
  • History of surgical treatment for obesity
  • History of heart disease
  • History of renal disease
  • Subjects with a history or clinically significant active disease of the gastrointestinal, cardiovascular, hepatic, neurological, renal, pancreatic, immunological, dermatological, endocrine, genitourinary or hematological system.
  • History or current diagnosis of acute or chronic pancreatitis
  • History of major depression, anxiety, suicidal behavior or attempts, or other psychiatric disorder requiring medical treatment
  • History of alcohol or illicit drug abuse including marijuana
  • Existence of any surgical or medical condition that, in the judgment of the Investigator, might interfere with the investigational product
  • Any history of clinically significant chronic liver disease

Sites / Locations

  • ProscientoRecruiting
  • Southwest General Healthcare CenterRecruiting
  • Combined Research OrlandoRecruiting
  • FDI Clinical ResearchRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm 9

Arm 10

Arm 11

Arm 12

Arm 13

Arm 14

Arm 15

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Group A1 - Single Ascending Dose

Group A2, Single Ascending Dose

Group A3, Single Ascending Dose

Group A4, Single Ascending Dose

Group B2 - Multiple Ascending Dose

Group B3 - Multiple Ascending Dose

Group B4 - Multiple Ascending Dose

Group B5 - Multiple Ascending Dose

Group B6 - Multiple Ascending Dose

Group A5, Single Ascending Dose

Group A6, Single Ascending Dose

Group A7, Single Ascending Dose

Group A8, Single Ascending Dose

Group B7 - Multiple Ascending Dose

Group B8 - Multiple Ascending Dose

Arm Description

DD01 Dose 1 (N=6) Placebo (N=2) Subcutaneous injection

DD01 Dose 2 (N=6) Placebo (N=2) Subcutaneous injection

DD01 Dose 3 (N=6) Placebo (N=2) Subcutaneous injection

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection

DD01 Dose 2 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks

DD01 Dose 3 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks

DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks

Outcomes

Primary Outcome Measures

Number of participants with treatment-related adverse events and serious adverse events
Number of participants with treatment-related adverse events and serious adverse events (TEAEs)
Number of participants with clinically significant abnormalities in clinical laboratory values
Number of participants with clinically significant abnormalities in clinical laboratory values
Number of participants with clinically significant abnormalities in physical examinations
Number of participants with clinically significant abnormalities in physical examinations
Number of participants with clinically significant abnormalities in vital signs
Number of participants with clinically significant abnormalities in vital signs
Blood Pressure assessed by 24-hour ambulatory blood pressure monitoring (ABPM)
Blood Pressure assessed by 24-hour ambulatory blood pressure monitoring (ABPM)
Heart Rate assessed by 24-hour ambulatory electrocardiography monitoring reader)
Heart Rate assessed by 24-hour ambulatory electrocardiography monitoring reader)
Number of participants with clinically significant abnormalities in 12-lead ECGs
Number of participants with clinically significant abnormalities in 12-lead ECGs

Secondary Outcome Measures

Maximum observed blood/plasma concentration of DD01
Maximum observed blood/plasma concentration (Cmax)
Maximum observed blood/plasma concentration of DD01
Maximum observed blood/plasma concentration (Cmax)
Time of the maximum observed blood/plasma concentration of DD01
Time of the maximum observed blood/plasma concentration (Tmax)
Time of the maximum observed blood/plasma concentration of DD01
Time of the maximum observed blood/plasma concentration (Tmax)
Apparent blood/plasma terminal elimination half life of DD01
Apparent blood/plasma terminal elimination half life (t1/2)
Apparent blood/plasma terminal elimination half life of DD01
Apparent blood/plasma terminal elimination half life (t1/2)
Termination elimination rate constant of DD01
Termination elimination rate constant (kel)
Termination elimination rate constant of DD01
Termination elimination rate constant (kel)
Apparent total blood/plasma clearance of DD01
Apparent total blood/plasma clearance (CL/F)
Apparent total blood/plasma clearance of DD01
Apparent total blood/plasma clearance (CL/F)
Apparent volume of distribution of DD01
Apparent volume of distribution(Vz/F)
Apparent volume of distribution of DD01
Apparent volume of distribution(Vz/F)
Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration of DD01
Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration (AUC0-t)
Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration of DD01
Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration (AUC0-t)
Area under the blood/plasma concentration time curve from time zero to 144 hours postdose of DD01
Area under the blood/plasma concentration time curve from time zero to 144 hours postdose (AUC0-144)
Area under the blood/plasma concentration time curve from time zero to 144 hours postdose of DD01
Area under the blood/plasma concentration time curve from time zero to 144 hours postdose (AUC0-144)
Area under the blood/plasma concentration time curve from time zero to 216 hours postdose of DD01
Area under the blood/plasma concentration time curve from time zero to 216 hours postdose (AUC0-216)
Area under the blood/plasma concentration time curve from time zero to 216 hours postdose of DD01
Area under the blood/plasma concentration time curve from time zero to 216 hours postdose (AUC0-216)
Area under the blood/plasma concentration time curve from time zero to 168 hours postdose of DD01
Part B only: Area under the blood/plasma concentration time curve from time zero to 168 hours postdose (AUC0-168)
Number of participants with antidrug antibodies (ADAs)
Number of participants with antidrug antibodies (ADAs)

Full Information

First Posted
March 19, 2021
Last Updated
May 3, 2022
Sponsor
Neuraly, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT04812262
Brief Title
A Phase 1 Study of DD01 in Overweight/Obese Subjects With T2DM and NAFLD
Official Title
A Phase 1, Randomized, Double-blind, Placebo-controlled, Single and Multiple Dose Study to Assess Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of DD01 in Overweight/Obese Subjects With T2DM and NAFLD
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 24, 2021 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Neuraly, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a Phase 1, first in human (FiH), randomized, double-blind, placebo-controlled, single ascending dose (SAD) and multiple ascending dose (MAD) study to investigate the safety, tolerability, PK and PD of DD01 administered by subcutaneous (SC) injection in overweight/obese subjects with type 2 diabetes (T2DM) and nonalcoholic fatty liver disease (NAFLD). The study will be conducted in 2 Parts (Part A and B), with up to 8 cohorts included in each part (Part A; Cohorts A1 to A8 and Part B; Cohorts B2 to B8).
Detailed Description
Part A (SAD): In Part A, subjects will receive a single dose of study drug, and the safety and efficacy of DD01 will be evaluated in overweight/obese subjects with T2DM. Part B (MAD): In Part B, subjects will receive once-weekly doses of the study drug for 4 weeks, and the safety and efficacy of DD01 will be evaluated in overweight/obese subjects with T2DM and NAFLD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity, Type2 Diabetes, NAFLD
Keywords
Liver Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Sequential Assignment
Model Description
Part A - Cohorts A1, A2, A3, A4, A5, A6, A7 & A8 Part B - Cohorts B2, B3, B4, B5, B6, B7 & B8
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A1 - Single Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 1 (N=6) Placebo (N=2) Subcutaneous injection
Arm Title
Group A2, Single Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 2 (N=6) Placebo (N=2) Subcutaneous injection
Arm Title
Group A3, Single Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 3 (N=6) Placebo (N=2) Subcutaneous injection
Arm Title
Group A4, Single Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection
Arm Title
Group B2 - Multiple Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 2 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks
Arm Title
Group B3 - Multiple Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 3 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks
Arm Title
Group B4 - Multiple Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks
Arm Title
Group B5 - Multiple Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks
Arm Title
Group B6 - Multiple Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks
Arm Title
Group A5, Single Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection
Arm Title
Group A6, Single Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection
Arm Title
Group A7, Single Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection
Arm Title
Group A8, Single Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection
Arm Title
Group B7 - Multiple Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks
Arm Title
Group B8 - Multiple Ascending Dose
Arm Type
Experimental
Arm Description
DD01 Dose 4 (N=6) Placebo (N=2) Subcutaneous injection once weekly for 4 weeks
Intervention Type
Drug
Intervention Name(s)
DD01
Intervention Description
The active of DD01 is a synthetic peptide, administered in a 1mL volume for injection.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo drug of DD01, administered in a 1mL volume for injection
Primary Outcome Measure Information:
Title
Number of participants with treatment-related adverse events and serious adverse events
Time Frame
Part A - 43 days
Title
Number of participants with treatment-related adverse events and serious adverse events (TEAEs)
Time Frame
Part B - 57 days
Title
Number of participants with clinically significant abnormalities in clinical laboratory values
Time Frame
Part A - 43 days
Title
Number of participants with clinically significant abnormalities in clinical laboratory values
Time Frame
Part B - 57 days
Title
Number of participants with clinically significant abnormalities in physical examinations
Time Frame
Part A - 43 days
Title
Number of participants with clinically significant abnormalities in physical examinations
Time Frame
Part B - 57 days
Title
Number of participants with clinically significant abnormalities in vital signs
Time Frame
Part A - 43 days
Title
Number of participants with clinically significant abnormalities in vital signs
Time Frame
Part B - 57 days
Title
Blood Pressure assessed by 24-hour ambulatory blood pressure monitoring (ABPM)
Time Frame
Part A - 43 days
Title
Blood Pressure assessed by 24-hour ambulatory blood pressure monitoring (ABPM)
Time Frame
Part B - 57 days
Title
Heart Rate assessed by 24-hour ambulatory electrocardiography monitoring reader)
Time Frame
Part A - 43 days
Title
Heart Rate assessed by 24-hour ambulatory electrocardiography monitoring reader)
Time Frame
Part B - 57 days
Title
Number of participants with clinically significant abnormalities in 12-lead ECGs
Time Frame
Part A - 43 days
Title
Number of participants with clinically significant abnormalities in 12-lead ECGs
Time Frame
Part B - 57 days
Secondary Outcome Measure Information:
Title
Maximum observed blood/plasma concentration of DD01
Description
Maximum observed blood/plasma concentration (Cmax)
Time Frame
Part A - 43 days
Title
Maximum observed blood/plasma concentration of DD01
Description
Maximum observed blood/plasma concentration (Cmax)
Time Frame
Part B - 57 days
Title
Time of the maximum observed blood/plasma concentration of DD01
Description
Time of the maximum observed blood/plasma concentration (Tmax)
Time Frame
Part A - 43 days
Title
Time of the maximum observed blood/plasma concentration of DD01
Description
Time of the maximum observed blood/plasma concentration (Tmax)
Time Frame
Part B - 57 days
Title
Apparent blood/plasma terminal elimination half life of DD01
Description
Apparent blood/plasma terminal elimination half life (t1/2)
Time Frame
Part A - 43 days
Title
Apparent blood/plasma terminal elimination half life of DD01
Description
Apparent blood/plasma terminal elimination half life (t1/2)
Time Frame
Part B - 57 days
Title
Termination elimination rate constant of DD01
Description
Termination elimination rate constant (kel)
Time Frame
Part A - 43 days
Title
Termination elimination rate constant of DD01
Description
Termination elimination rate constant (kel)
Time Frame
Part B - 57 days
Title
Apparent total blood/plasma clearance of DD01
Description
Apparent total blood/plasma clearance (CL/F)
Time Frame
Part A - 43 days
Title
Apparent total blood/plasma clearance of DD01
Description
Apparent total blood/plasma clearance (CL/F)
Time Frame
Part B - 57 days
Title
Apparent volume of distribution of DD01
Description
Apparent volume of distribution(Vz/F)
Time Frame
Part A - 43 days
Title
Apparent volume of distribution of DD01
Description
Apparent volume of distribution(Vz/F)
Time Frame
Part B - 57 days
Title
Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration of DD01
Description
Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration (AUC0-t)
Time Frame
Part A - 43 days
Title
Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration of DD01
Description
Area under the blood/plasma concentration time curve from time zero to the time of the last quantifiable concentration (AUC0-t)
Time Frame
Part B - 57 days
Title
Area under the blood/plasma concentration time curve from time zero to 144 hours postdose of DD01
Description
Area under the blood/plasma concentration time curve from time zero to 144 hours postdose (AUC0-144)
Time Frame
Part A - 43 days
Title
Area under the blood/plasma concentration time curve from time zero to 144 hours postdose of DD01
Description
Area under the blood/plasma concentration time curve from time zero to 144 hours postdose (AUC0-144)
Time Frame
Part B - 57 days
Title
Area under the blood/plasma concentration time curve from time zero to 216 hours postdose of DD01
Description
Area under the blood/plasma concentration time curve from time zero to 216 hours postdose (AUC0-216)
Time Frame
Part A - 43 days
Title
Area under the blood/plasma concentration time curve from time zero to 216 hours postdose of DD01
Description
Area under the blood/plasma concentration time curve from time zero to 216 hours postdose (AUC0-216)
Time Frame
Part B - 57 days
Title
Area under the blood/plasma concentration time curve from time zero to 168 hours postdose of DD01
Description
Part B only: Area under the blood/plasma concentration time curve from time zero to 168 hours postdose (AUC0-168)
Time Frame
Part B - 57 days
Title
Number of participants with antidrug antibodies (ADAs)
Time Frame
Part A - 43 days
Title
Number of participants with antidrug antibodies (ADAs)
Time Frame
Part B - 57 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Part A Inclusion Criteria: Type 2 diabetes ≥ 12 months. Treatment with diet and exercise or metformin monotherapy on stable dose for 3 months prior to screening HbA1c ≤ 10%). Body Mass Index (BMI) ≥ 25 and ≤ 40.0 kg/m2 Part B Inclusion Criteria Type 2 diabetes ≥ 12 months. Treatment with diet and exercise or metformin monotherapy on stable dose for 3 months prior to screening HbA1c ≤ 10% BMI ≥ 30 kg/m2 and ≤ 40.0 kg/m2 Waist circumference ≤ 57 inches Controlled attenuation parameter by FibroScan Liver fat fraction ≥ 10% by magnetic resonance imaging (MRI) Part A Exclusion Criteria: History of type 1 diabetes mellitus (T1DM) History of acute proliferative retinopathy or maculopathy, severe gastroparesis, and/or severe neuropathy, in particular autonomic neuropathy, as judged by the Investigator. Uncontrolled hypertension Treatment with antihypertensive medication and statins not stable during the past 2 months prior to screening Treatment with thyroid hormones not stable during the past 3 months prior to screening History of any weight control treatment, including over-the-counter and herbal medication and supplements, or any medication with a labeled indication for weight loss or weight gain within 3 months prior to screening History of surgical treatment for obesity History of heart disease History of renal disease History or current diagnosis of acute or chronic pancreatitis or factors for pancreatitis, such as a history of cholelithiasis (without cholecystectomy) or alcohol abuse A history of or active chronic liver disease due to alcohol, auto-immune, HIV, HBV or active HCV-infection or NASH History of major depression, anxiety, suicidal behavior or attempts, or other psychiatric disorder requiring medical treatment Personal or family history of medullary thyroid carcinoma (MTC) or a genetic condition that predispose to MTC (i.e., multiple endocrine neoplasia type 2) Administration of Vaccines/Immunizations within 14 days prior to first dosing or if scheduled during the study. Vaccination for COVID-19 is allowed during the study if a washout period of 5 days after vaccine administration is followed before dosing. History of any major surgery within 6 months prior to screening Participation in any other clinical interventional study receiving active treatment within 30 days or 5 half-lives prior to screening, whichever is longer History of alcohol or illicit drug abuse including marijuana Existence of any surgical or medical condition that, in the judgment of the Investigator, might interfere with the investigational product PART B Exclusion Criteria History of type 1 diabetes mellitus (T1DM) History of acute proliferative retinopathy or maculopathy, severe gastroparesis, and/or severe neuropathy, in particular autonomic neuropathy, as judged by the Investigator Uncontrolled hypertension (treatment with medications must be stable) History of any weight control treatment History of surgical treatment for obesity History of heart disease History of renal disease Subjects with a history or clinically significant active disease of the gastrointestinal, cardiovascular, hepatic, neurological, renal, pancreatic, immunological, dermatological, endocrine, genitourinary or hematological system. History or current diagnosis of acute or chronic pancreatitis History of major depression, anxiety, suicidal behavior or attempts, or other psychiatric disorder requiring medical treatment History of alcohol or illicit drug abuse including marijuana Existence of any surgical or medical condition that, in the judgment of the Investigator, might interfere with the investigational product Any history of clinically significant chronic liver disease
Facility Information:
Facility Name
Prosciento
City
Chula Vista
State/Province
California
ZIP/Postal Code
91911
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Robyn Rodriguez
Phone
619-799-4818
Email
robyn.rodriguez@prosciento.com
Facility Name
Southwest General Healthcare Center
City
Fort Myers
State/Province
Florida
ZIP/Postal Code
33907
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brian Warnsky
Phone
407-476-0514
Email
brian.swghcc@gmail.com
First Name & Middle Initial & Last Name & Degree
Jose E Rodriguez
Facility Name
Combined Research Orlando
City
Orlando
State/Province
Florida
ZIP/Postal Code
32807
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yenilady Estevez
Phone
407-440-4493
Email
yenilady@clinicaltrialsorlando.com
Facility Name
FDI Clinical Research
City
San Juan
ZIP/Postal Code
00927
Country
Puerto Rico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Digmarie Rivera
Phone
787-722-1248
Email
drivera@fdipr.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Phase 1 Study of DD01 in Overweight/Obese Subjects With T2DM and NAFLD

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