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A Study of Concurrent Stereotactic Body Radiotherapy With Opdualag in Metastatic Uveal Melanoma

Primary Purpose

Uveal Melanoma

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
stereotactic body radiotherapy
Immunotherapy
Sponsored by
California Pacific Medical Center Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Uveal Melanoma focused on measuring metastatic

Eligibility Criteria

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

Inclusion Criteria:

  • measurable metastatic uveal melanoma.
  • No concomitant therapy.
  • Prior PD1 or tebendafesp allowed.
  • Performance status 0-1.
  • No active Hepatitis B.
  • No known HIV infection.
  • WBC>2000, ANC>1500, Hgb >8.
  • Creatinine < 3 x ULN.
  • AST & ALT < 2.5 x ULN Bilirubin < 2 x ULN.
  • Albumin >2.9

Exclusion Criteria:

  • Liver tumor volume > 50%.
  • Active CNS metastases.
  • Pregnancy.
  • Prior therapy with ipilimumab or other CTLA-4 inhibitor.
  • Certain autoimmune diseases.
  • Previous liver embolization or radiation.
  • Use of systemic steroids

Sites / Locations

  • California Pacific Medical Center Research InstituteRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

one arm

Arm Description

see below

Outcomes

Primary Outcome Measures

safety and tolerability of the therapy
toxicity measured by CTAE graded 3-5 toxicities

Secondary Outcome Measures

Response rate
iRECIST defined response rates

Full Information

First Posted
October 5, 2021
Last Updated
December 2, 2022
Sponsor
California Pacific Medical Center Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05077280
Brief Title
A Study of Concurrent Stereotactic Body Radiotherapy With Opdualag in Metastatic Uveal Melanoma
Official Title
A Phase II Study of Concurrent Stereotactic Body Radiotherapy With Relatlimab and Nivolumab in Patients With Metastatic Uveal Melanoma
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 20, 2021 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
March 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
California Pacific Medical Center Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a phase 2 trial of concurrent stereotactic radiation therapy (SBRT) with immunotherapy with relatlimab and nivolumab for up to two years. SBRT will be given in three doses of 15Gy each to 1-5 separate metastases. Opdualag (nivolumab 480mg and relatlimab 160mg) will be given every 4 weeks for two years
Detailed Description
Metastatic uveal melanoma has no standard therapy, but there is evidence that both radiation therapy and immunotherapy may be helpful and may be synergistic. This is a phase 2 trial of concurrent stereotactic radiation therapy (SBRT) with immunotherapy with Opdualag (nivolumab 480mg and relatlimab 160mg) for up to two years. SBRT will be given in three doses of 15Gy each to 1-5 separate metastases, limiting the total dosage to 700cc's of normal liver to <15Gy. Opdualag (nivolumab 480mg and relatlimab 160mg) will be given every 4 weeks for two years. Objectives are to determine the safety and tolerability, and iRECIST will be used to determine responses.We will treat up to 50 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Uveal Melanoma
Keywords
metastatic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
one arm
Arm Type
Experimental
Arm Description
see below
Intervention Type
Radiation
Intervention Name(s)
stereotactic body radiotherapy
Intervention Description
Stereotactic Body radiotherapy will be given to 1-5 target metastases in 3 doses over 8 days or less. Each dose will be 15Gy for a total dose of 45GY
Intervention Type
Drug
Intervention Name(s)
Immunotherapy
Intervention Description
Opdualag (nivolumab 480mg and relatlimab 160mg) will be given every 4 weeks for two years
Primary Outcome Measure Information:
Title
safety and tolerability of the therapy
Description
toxicity measured by CTAE graded 3-5 toxicities
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Response rate
Description
iRECIST defined response rates
Time Frame
5 years
Other Pre-specified Outcome Measures:
Title
Progression-free survival
Description
survival without progressive cancer
Time Frame
5 years
Title
Overall survival
Description
survival
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: measurable metastatic uveal melanoma. No concomitant therapy. Prior PD1 or tebendafesp allowed. Performance status 0-1. No active Hepatitis B. No known HIV infection. WBC>2000, ANC>1500, Hgb >8. Creatinine < 3 x ULN. AST & ALT < 2.5 x ULN Bilirubin < 2 x ULN. Albumin >2.9 Exclusion Criteria: Liver tumor volume > 50%. Active CNS metastases. Pregnancy. Prior therapy with Opdualag or relatlimab Certain autoimmune diseases. Previous liver embolization or radiation. Use of systemic steroids
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Madeline Decker
Phone
4156006000
Email
KimKB@sutterhealth.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David R Minor, MD
Organizational Affiliation
California Pacific Med Center Research Inst.
Official's Role
Study Chair
Facility Information:
Facility Name
California Pacific Medical Center Research Institute
City
San Francisco
State/Province
California
ZIP/Postal Code
94115
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Madeline Decker
Phone
415-600-3613
Email
KimB@sutterhealth.org
First Name & Middle Initial & Last Name & Degree
Kevin B Kim, M.D.

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Study of Concurrent Stereotactic Body Radiotherapy With Opdualag in Metastatic Uveal Melanoma

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