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Completed Phase 2 Interventional

The TIME-2 Study: A Phase 2 Study of AKB-9778, a Novel Tie-2 Activator, in Patients With Diabetic Macular Edema

ClinicalTrials.gov ID: NCT02050828

Public ClinicalTrials.gov record NCT02050828. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 4:16 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Active-Controlled, Double-Masked, Multi-Center Study to Assess the Safety and Efficacy of Daily Subcutaneous AKB-9778 Administered for 3 Months, as Monotherapy or Adjunctive to Ranibizumab, in Subjects With Diabetic Macular Edema

Study identification

NCT ID
NCT02050828
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Aerpio Therapeutics
Industry
Enrollment
144 participants

Conditions and interventions

Interventions

  • AKB-9778 Drug
  • ranibizumab Drug
  • Placebo Drug
  • Sham Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2013
Primary completion
Mar 31, 2015
Completion
Apr 30, 2015
Last update posted
Mar 15, 2017

2014 – 2015

United States locations

U.S. sites
39
U.S. states
19
U.S. cities
38
Facility City State ZIP Site status
Not listed Pheonix Arizona 85014
Not listed Pheonix Arizona 85020
Not listed Tucson Arizona 85704
Not listed Arcadia California 91007
Not listed Bakersfield California 93309
Not listed Beverly Hills California 90211
Not listed Palm Desert California 92260
Not listed Sacramento California 95819
Not listed Santa Ana California 92705
Not listed Santa Barbara California 93103
Not listed Golden Colorado 80401
Not listed Boynton Beach Florida 33426
Not listed Fort Lauderdale Florida 33334
Not listed Fort Myers Florida 33912
Not listed Miami Florida 33126
Not listed Sarasota Florida 34239
Not listed Stuart Florida 34994
Not listed Winter Haven Florida 33880
Not listed Baltimore Maryland 21287
Not listed Jackson Michigan 49202
Not listed Omaha Nebraska 68198
Not listed Reno Nevada 89502
Not listed Rochester New York 14620
Not listed Charlotte North Carolina 28210
Not listed Cincinnati Ohio 45242
Not listed Cleveland Ohio 44195
Not listed Portland Oregon 97210
Not listed Florence South Carolina 29501
Not listed Rapid City South Dakota 57701
Not listed Nashville Tennessee 37203
Not listed Abilene Texas 79606
Not listed Austin Texas 78705
Not listed Fort Worth Texas 76102
Not listed Houston Texas 77030
Not listed McAllen Texas 78503
Not listed San Antonio Texas 78240
Not listed Salt Lake City Utah 84107
Not listed Warrenton Virginia 20186
Not listed Bellevue Washington 98004

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02050828, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 15, 2017 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02050828 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →