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Completed Phase 1Phase 2 Interventional

Study of LYC-55716 in Adult Subjects With Locally Advanced or Metastatic Cancer

ClinicalTrials.gov ID: NCT02929862

Public ClinicalTrials.gov record NCT02929862. 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 Sep 7, 2026, 4:21 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 1/2A Multicenter, Open-Label Study of LYC-55716 in Adult Subjects With Locally Advanced or Metastatic Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 1/2A study designed to evaluate the safety and tolerability of increased repeated doses of LYC-55716 in subjects with locally advanced or metastatic solid tumors.

Study identification

NCT ID
NCT02929862
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Lycera Corp.
Industry
Enrollment
119 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Nov 30, 2016
Primary completion
May 30, 2019
Completion
May 30, 2019
Last update posted
Sep 24, 2019

2016 – 2019

United States locations

U.S. sites
20
U.S. states
17
U.S. cities
20
Facility City State ZIP Site status
Lycera Investigational Site Huntsville Alabama 35805
Lycera Investigational Site Sacramento California 95817
Lycera Investigational Site Washington D.C. District of Columbia 20007
Lycera Investigational Site Sarasota Florida 34232
Lycera Investigational Site Atlanta Georgia 30322
Lycera Investigational Site Augusta Georgia 30912
Lycera Investigational Site Chicago Illinois 60611
Lycera Investigational Site Saint Cloud Minnesota 56303
Lycera Investigational Site Omaha Nebraska 68130
Lycera Investigational Site New York New York 10016
Lycera Investigational Site Durham North Carolina 27710
Lycera Investigational Site Oklahoma City Oklahoma 73104
Lycera Investigational Site Portland Oregon 97213
Lycera Investigational Site Philadelphia Pennsylvania 19111
Lycera Investigational Site Greenville South Carolina 29605
Lycera Investigational Site Nashville Tennessee 37203
Lycera Investigational Site Dallas Texas 75230
Lycera Investigational Site San Antonio Texas 78229
Lycera Investigational Site Charlottesville Virginia 22908
Lycera Investigational Site Fairfax Virginia 22031

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 NCT02929862, 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 Sep 24, 2019 · Synced Sep 7, 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 NCT02929862 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →