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

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ClinicalTrials.gov Identifier: NCT02929862
Recruitment Status : Completed
First Posted : October 11, 2016
Last Update Posted : September 25, 2019
Information provided by (Responsible Party):
Lycera Corp.

Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Cancer Drug: LYC-55716 Phase 1 Phase 2

Detailed Description:

Approximately 30 subjects across approximately 5 United States (US) sites will be enrolled in the Phase 1 portion of the study and approximately 69-84 subjects across approximately 15 US sites will be enrolled in the Phase 2A portion of the study.

The Phase 1 portion of the study will follow a 3 + 3 dose-escalation design to evaluate twice-daily (BID) administration of LYC-55716 for DLTs and to determine the MTD and the RP2D for further assessment in Phase 2A. A treatment cycle will consist of 28 days of treatment and subjects may continue to receive subsequent cycles of therapy as long as they do not have clinically significant progressive disease.

In the Phase 2A portion of the study, 69-84 subjects with locally advanced or metastatic solid tumors considered most likely to be responsive to a RORγ agonist will be enrolled and treated at the MTD or RP2D.

Six cohorts of subjects with advanced cancer will be enrolled. Cohorts 1 to 3 will enroll 14 to 19 subjects per cohort. Tumor types include NSCLC (Cohort 1); gastric, esophageal and G-E junction adenocarcinoma (Cohort 2); and SCCHN (Cohort 3). Cohorts 4 to 6 will enroll up to 9 subjects per cohort. Tumor types include ovarian carcinoma (Cohort 4), renal cell carcinoma (Cohort 5), and urothelial carcinoma (Cohort 6).

Primary Study Objectives

Phase 1

  • Evaluate the safety and tolerability of LYC-55716
  • Determine the maximum tolerated dose (MTD) and the recommended Phase 2 dose (RP2D)

Phase 2A

• Determine the objective response rate according to response evaluation criteria in solid tumors (RECIST) v1.1.

Secondary Study Objectives

Phase 1

  • Evaluate the activity of LYC-55716 by objective response according to RECIST v1.1.
  • Determine the durability of any observed objective response

Phase 2A

  • Determine the duration of response
  • Determine progression-free survival (PFS) and overall survival (OS)
  • Determine suitability of the RP2D for further study
  • Characterize the pharmacokinetics (PK) of LYC-55716

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 119 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1/2A Multicenter, Open-Label Study of LYC-55716 in Adult Subjects With Locally Advanced or Metastatic Cancer
Study Start Date : December 2016
Actual Primary Completion Date : May 31, 2019
Actual Study Completion Date : May 31, 2019

Arm Intervention/treatment
Experimental: Single Agent 55716 Drug: LYC-55716
For Phase 1, increasing doses of oral 55716 given BID for a 28 day cycle. For Phase 2A, the RP2D will be administered to patients for 28 day cycles.

Primary Outcome Measures :
  1. Assess Tumor Activity [ Time Frame: 8 weeks ]
    Evaluated according to RECIST v1.1

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Subject is male or female and at least 18 years of age.
  • Histological or cytological confirmation of advanced unresectable solid tumors, including those subjects who have progressed on standard anticancer therapy and for whom no further therapy that confers clinical benefit is available.
  • Subject has an Eastern Cooperative Oncology Group (ECOG) score of 0 1 or Karnofsky Performance Status Score ≥ 70.
  • Subject has a life expectancy of at least 12 weeks.
  • Subject has adequate organ function as determined by the following laboratory values:

    • Absolute Neutrophil Count* ≥ 1,500/mm3 (≥ 1.5 x 109/L)
    • Platelets* ≥ 100,000/mm3 (≥ 100 x 109/L)
    • Lymphocytes ≥ 0.5 x 109/L
    • Hemoglobin* > 9.0 g/dL
    • Serum Creatinine or Creatinine Clearance** ≤ 1.5 x ULN, > 50 mL/min
    • Total Serum Bilirubin ≤ 1.5 x ULN (< 3.0 mg/dL if subject has Gilbert's syndrome)
    • Liver Transaminases (ALT/AST) ≤ 2.5 x ULN, ≤ 5.0 x ULN if liver metastases present

      • (* = without ongoing growth factor or transfusion support)
      • (** = calculated by Cockcroft and Gault's formula)
      • (ALT = alanine aminotransferase, AST = aspartate aminotransferase, ULN = upper limit of normal)

Exclusion Criteria:

  • Subject has received an investigational drug in the 28 day period before the first dose of study drug (or within 5 half-lives if longer) or is currently participating in another interventional clinical trial.
  • Subject has known symptomatic brain metastases or leptomeningeal involvement as assessed by CT scan or MRI. Subjects with stable asymptomatic brain metastases or leptomeningeal disease are eligible if they have not required new treatments for this disease in a 28 day period before the first dose of study drug, and anticonvulsants and steroids have not been administered for a period of 2 weeks prior to the first dose of study drug.
  • Subject has not recovered from adverse reactions to prior cancer treatment or procedures (surgery, chemotherapy, immunotherapy, radiation therapy) to Common Terminology Criteria for Adverse Events (CTCAE) Grade 2 or better.
  • Subject has a previous (within 5 years) or current malignancy other than the target cancer with the exception of curatively treated local tumors such as carcinoma in situ of the breast or cervix, basal or squamous cell carcinoma of the skin, or prostate cancer with Gleason Grade < 6 and prostate-specific antigen within normal range.

Modifications to Eligibility Criteria for the following specific tumor types:

Phase 2A will be limited to enrolling the following tumor types:

  • Gastric, Esophageal, and G-E Junction Adenocarcinoma
  • Ovarian Carcinoma
  • Renal Cell Carcinoma
  • Urothelial Carcinoma

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02929862

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United States, Alabama
Lycera Investigational Site
Huntsville, Alabama, United States, 35805
United States, California
Lycera Investigational Site
Sacramento, California, United States, 95817
United States, District of Columbia
Lycera Investigational Site
Washington, District of Columbia, United States, 20007
United States, Florida
Lycera Investigational Site
Sarasota, Florida, United States, 34232
United States, Georgia
Lycera Investigational Site
Atlanta, Georgia, United States, 30322
Lycera Investigational Site
Augusta, Georgia, United States, 30912
United States, Illinois
Lycera Investigational Site
Chicago, Illinois, United States, 60611
United States, Minnesota
Lycera Investigational Site
Saint Cloud, Minnesota, United States, 56303
United States, Nebraska
Lycera Investigational Site
Omaha, Nebraska, United States, 68130
United States, New York
Lycera Investigational Site
New York, New York, United States, 10016
United States, North Carolina
Lycera Investigational Site
Durham, North Carolina, United States, 27710
United States, Oklahoma
Lycera Investigational Site
Oklahoma City, Oklahoma, United States, 73104
United States, Oregon
Lycera Investigational Site
Portland, Oregon, United States, 97213
United States, Pennsylvania
Lycera Investigational Site
Philadelphia, Pennsylvania, United States, 19111
United States, South Carolina
Lycera Investigational Site
Greenville, South Carolina, United States, 29605
United States, Tennessee
Lycera Investigational Site
Nashville, Tennessee, United States, 37203
United States, Texas
Lycera Investigational Site
Dallas, Texas, United States, 75230
Lycera Investigational Site
San Antonio, Texas, United States, 78229
United States, Virginia
Lycera Investigational Site
Charlottesville, Virginia, United States, 22908
Lycera Investigational Site
Fairfax, Virginia, United States, 22031
Sponsors and Collaborators
Lycera Corp.
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Responsible Party: Lycera Corp.
ClinicalTrials.gov Identifier: NCT02929862    
Other Study ID Numbers: LYC-55716-1001
First Posted: October 11, 2016    Key Record Dates
Last Update Posted: September 25, 2019
Last Verified: May 2018
Additional relevant MeSH terms:
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Neoplasm Metastasis
Neoplastic Processes
Pathologic Processes