Intrahepatic Delivery of SD-101 by Pressure-Enabled Regional Immuno-oncology (PERIO), With Checkpoint Blockade in Adults With Metastatic Uveal Melanoma

• ClinicalTrials.gov Identifier: NCT04935229
• Recruitment Status: Recruiting
• First Posted: June 22, 2021
• Last Update Posted: January 31, 2023
• Sponsor: TriSalus Life Sciences, Inc.
• Information provided by (Responsible Party): TriSalus Life Sciences, Inc.

Study Description

Brief Summary:

This study is an open-label, phase 1/1b study of the pressure-enabled hepatic artery infusion of SD-101, a TLR 9 agonist, alone or in combination with intravenous checkpoint blockade in adults with metastatic uveal melanoma.

Condition or disease	Intervention/treatment	Phase
Metastatic Uveal Melanoma in the Liver	Drug: SD-101; Biological: Nivolumab; Biological: Ipilimumab; Biological: Nivolumab and Relatlimab	Phase 1

Detailed Description:

In the Sentinel Cohort, patients will receive 2 SD-101 infusions (2 weeks apart) with assessments for toxicity prior to escalating from the first dose level (0.5 mg) to the second dose level (2 mg). In the absence of dose-limiting toxicities (DLTs), each patient will be eligible to transition into Cohort A.

In Cohorts A-C and Phase 1b, patients will receive 2 cycles of SD-101. Each cycle consists of 3 consecutive weekly infusions. Escalating doses of SD-101 will be administered alone (Cohort A), together with nivolumab (Cohort B), together with combined ipilimumab and nivolumab (Cohort C), or together with nivolumab and relatlimab (Cohort C1 - optional). Cohorts B and C will begin dosing at the minimum anticipated biological effect level (MABEL(2mg SD-101)).

An optional Cohort D may be opened to explore the combination of one or more of the following three CPI regimens with a modified SD-101 dosing schedule with only 2 weekly SD-101 infusions per cycle for 2 cycles:

1. Single-agent nivolumab IV at 480mg every 4 weeks;
2. IV ipilimumab 3mg/kg and IV nivolumab 1mg/kg every 3 weeks for 4 doses each followed thereafter by nivolumab 480mg IV every 4 weeks;
3. Nivolumab 480mg and relatlimab 160mg IV every 4 weeks.

Following determination of the recommended MTD or optimal dose of SD-101 for PEDD/HAI and which checkpoint inhibitor (CPI) regimen(s) are tolerated, the study will progress to Phase 1b. Patients in Phase 1b will receive the SD-101 dose selected from Phase 1 together with systemic single- or double-agent checkpoint blockade. The choice of single- or double-agent CPI therapy together with SD-101 for Phase 1b will consider safety data in addition to response rates from Cohorts B and C in Phase 1.

Patients enrolled into the main study are eligible to enroll into an optional imaging sub-study investigating the use of 89Zr-Df-crefmirlimab, a biologic PET radioligand for detecting CD8+ T cell lymphocytes. 89Zr-Df-crefmirlimab will be administered by IV at screening and again prior to C2D1 procedures. A PET scan is conducted within 72 hours following the tracer infusion.

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 80 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment

Intervention Model Description

Sentinel Cohort: Two doses of SD-101 (0.5mg and 2mg) administered 2 weeks apart via PEDD/HAI using the TriNav device.

Cohorts A, B, C, and Phase 1b: Three weekly doses of SD-101 (given over two 52-day cycles) in dose-escalation fashion (2mg, 4mg, 8mg-optional) via PEDD/HAI using the TriNav device.

Cohort D (optional): Two weekly doses of SD-101 (given over two 52-day cycles) via PEDD/HAI using the TriNav device.

• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Phase 1/1b, Open-Label Study of the Pressure-Enabled Hepatic Artery Infusion of SD-101, a TLR9 Agonist, Alone or in Combination With Intravenous Checkpoint Blockade in Adults With Metastatic Uveal Melanoma
• Actual Study Start Date: August 2, 2021
• Estimated Primary Completion Date: September 2024
• Estimated Study Completion Date: January 2025

Arms and Interventions

Arm

Intervention/treatment

Experimental: SD-101; 3 weekly doses of SD-101 given via hepatic artery infusion over 2 cycles

Drug: SD-101; SD-101 doses will be delivered via hepatic artery infusion using pressure enabled drug delivery using the TriNav device; Biological: Nivolumab; During Cohort B, nivolumab will be administered together with SD-101 and during Cohort C, it will be administered with ipilimumab and SD-101; Other Name: Opdivo; Biological: Ipilimumab; During Cohort C, ipilimumab will be administered together with nivolumab and SD-101; Other Name: Yervoy; Biological: Nivolumab and Relatlimab; During optional Cohort C1, nivolumab and relatlimab will be administered with SD-101; Other Name: Opdualag

Outcome Measures

Primary Outcome Measures :

1. Phase 1: To Determine the Safety of SD-101 Alone, in Combination with Nivolumab, and in Combination with Both Nivolumab and Ipilimumab [ Time Frame: 12 months ]
   As a measure of safety, adverse events will be graded according to CTCAE v5.0.
2. Phase 1: To Determine the Maximum Tolerable Dose (MTD) or Optimal Dose of SD-101 alone, in Combination with Nivolumab, and in Combination with Both Nivolumab and Ipilimumab [ Time Frame: 12 months ]
   A standard 3+3 dose-escalation design will be employed to determine the MTD or optimal dose.
3. Phase 1b: To Assess Overall Response Rate (ORR) [ Time Frame: 12 months ]
   As a measure of activity, ORR will be assessed. ORR will be assessed using Response Evaluation Criteria in Solid Tumours (RECIST) v1.1.
4. Phase 1b: To Assess Overall Survival (OS) [ Time Frame: 12 months ]
   As a measure of activity, OS will be assessed. The events for the assessment of 12-month OS are death events.

Secondary Outcome Measures :

1. Phase 1: Determination of Single vs. Dual-agent CPI in Phase 1b using CTCAE v5.0 [ Time Frame: 6 months ]
   The choice of single- or dual-agent CPI therapy together with SD-101 for Phase 1b will consider AEs/SAEs per CTCAE v5.0.
2. Phase 1: Determination of Single vs. Dual-agent CPI in Phase 1b using RECIST v1.1 [ Time Frame: 6 months ]
   The choice of single- or dual-agent CPI therapy together with SD-101 for Phase 1b will consider response rates per RECIST v1.1 from Cohorts B and C in Phase 1.
3. Phase 1b: To Assess Treatment-Emergent Adverse Events of the Chosen MTD or Optimal Dose of SD-101 in Combination with CPI [ Time Frame: 6 months ]
   As a measure of safety, adverse events will be graded according to CTCAE v5.0.
4. Phase 1b: Assess Preliminary Efficacy in Terms of iRECIST for Immune Based Therapeutics [ Time Frame: 12 months ]
   As a measure of activity, iRECIST will be utilized to determine ORR.
5. Phase 1b: Assess Preliminary Efficacy in Terms of modified RECIST (mRECIST) for Immune Based Therapeutics [ Time Frame: 12 months ]
   As a measure of activity, mRECIST will be utilized to determine ORR.
6. Phase 1b: Assess Preliminary Efficacy in Terms of RECIST v1.1 for Immune Based Therapeutics [ Time Frame: 12 months ]
   As a measure of activity, RECIST 1.1 will be utilized to determine hepatic-specific response rate (HRR).
7. Phase 1b: Assess Preliminary Efficacy in Terms of RECIST v1.1 for Immune Based Therapeutics [ Time Frame: 12 months ]
   As a measure of activity, RECIST 1.1 will be utilized to determine duration of response (DOR).
8. Phase 1b: Assess Preliminary Efficacy in Terms of RECIST v1.1 for Immune Based Therapeutics [ Time Frame: 12 months ]
   As a measure of activity, RECIST 1.1 will be utilized to determine overall progression-free survival (PFS).
9. Phase 1b: Assess Preliminary Efficacy in Terms of RECIST v1.1 for Immune Based Therapeutics [ Time Frame: 12 months ]
   As a measure of activity, RECIST 1.1 will be utilized to determine clinical benefit (complete response [CR] + partial response [PR] + stable disease [SD]).

Eligibility Criteria

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

Criteria

Inclusion Criteria:

1. Male or female, age ≥18 years of age at screening
2. Able to understand the study and provide written informed consent prior to any study procedures
3. Has histologically or cytologically confirmed metastatic UM with liver-only or liver dominant disease. Liver-dominant disease will be defined as intrahepatic metastases representing the largest fraction of disease relative to other organs.
4. Has not received prior cytotoxic chemotherapy, targeted therapy, or external radiation therapy within 14 days prior to screening
5. Has not received therapy with prior immunological checkpoint blockade within 21 days before the first dose of study intervention and has no ongoing immune-mediated AEs Grade 2 or higher
6. Has not ever received prior embolic HAI therapy with permanent embolic material Note: Previous embolic HAI therapy with permanent embolic material will not be exclusionary if following this therapy, the target vessels are not occluded and the liver segments containing target tumors are perfused based on the patient's screening CT/MRI.
7. Prior surgical resection or radiofrequency ablation of oligometastatic liver disease is allowed on both the Phase 1 and Phase 1b portions of this study. Liver lesions that received ablative therapies should not be considered target lesions unless they have clearly progressed since the therapy.
8. Has no prior history of or other concurrent malignancy unless the malignancy is clinically insignificant, no ongoing treatment is required, and the patient is clinically stable
9. Has measurable disease in the liver according to RECIST v.1.1 criteria
10. Has an ECOG PS of 0-1 at screening
11. Has a life expectancy of >3 months at screening as estimated by the investigator
12. Has a QTc interval ≤480 msec
13. All associated clinically significant (in the judgment of the investigator) drug-related toxicity from previous cancer therapy must be resolved (to Grade ≤1 or the patient's pretreatment level) prior to study treatment administration (Grade 2 alopecia and endocrinopathies controlled on replacement therapy are allowed)

14. Has adequate organ function at screening as evidenced by:

    • Platelet count >100,000/μL
    • Hemoglobin ≥8.0 g/dL
    • White blood cell count (WBC) >2,000/μL
    • Serum creatinine ≤2.0 mg/dL unless the measured creatinine clearance is ≥30 mL/min calculated by Cockcroft-Gault formula.
    • Total and direct bilirubin ≤2.0 × the upper limit of normal (ULN) and alkaline phosphatase ≤5 × ULN. For patients with documented Gilbert's disease, total bilirubin up to 3.0 mg/dL is allowed.
    • ALT and AST ≤5 × ULN
    • Prothrombin time/International Normalized Ratio (INR) or activated partial thromboplastin time (aPTT) test results at screening ≤1.5 × ULN (this applies only to patients who do not receive therapeutic anticoagulation; patients receiving therapeutic anticoagulation should be on a stable dose for at least 4 weeks prior to the first dose of study intervention) Note: Laboratory tests with exclusionary results judged by the investigator as not compatible with the patient's clinical status may be repeated once for eligibility purposes.

15. Females of childbearing potential must be nonpregnant and nonlactating, or post-menopausal, and have a negative serum human chorionic gonadotropin (hCG) pregnancy test result at screening and a negative urine or serum pregnancy test prior to the first dose of study intervention.

    • Females of childbearing potential must agree to abstain from sexual activity with nonsterilized male partners, or if sexually active with a nonsterilized male partner must agree to use highly effective methods of contraception from screening, throughout the study and agree to continue using such precautions for 100 days after the final dose of study intervention.
    • Nonsterilized males who are sexually active with a female of childbearing potential must agree to use effective methods of contraception and avoid sperm donation from Day 1, throughout the study, and for 30 days after the final dose of study intervention.

Exclusion Criteria:

1. Has received chemotherapy or an investigational agent within 14 days (or 5 half-lives, whichever is shorter) before screening
2. Has active, untreated brain metastasis
3. Active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.
4. Has portal vein thrombosis, or severe portal hypertension as defined by a history of variceal hemorrhage or active ascites accumulation
5. Has more than 2/3 parenchymal replacement by tumor of both liver lobes

6. Phase 1 and Phase 1b:

   1. Has Child-Pugh Class B or C cirrhosis, or
   2. Has experienced a Grade 3 or higher immune-related AE from prior CPI therapy that has not recovered to Grade 1 for a minimum of 14 days prior to administration of SD-101 or CPI, or
   3. Is unable to be temporarily removed from chronic anticoagulation therapy, or
   4. Has a history of bleeding disorders
7. Has active coronavirus disease 2019 (COVID-19), other severe infection, including a liver infection, within 2 weeks before the first dose of study drug, or uncontrolled human immunodeficiency virus (HIV) infection at screening
8. Has had bacterial pneumonia within 8 weeks of first dose of study drug
9. Has active, known, or suspected autoimmune disease or immune-mediated disease. Type I diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders (such as vitiligo, psoriasis or alopecia) not requiring systemic treatment or conditions not expected to recur in the absences of an external trigger are not exclusionary.
10. Is receiving systemic steroid therapy >10 mg of prednisone daily or equivalent or any other immunosuppressive medication at any dose level. Local steroid therapies (e.g., otic, ophthalmic, intra-articular or inhaled medications) are acceptable.
11. Has significant concurrent or intercurrent illness, psychiatric disorder, or alcohol or chemical dependence that would, in the opinion of the Investigator and/or Medical Monitor, compromise their safety or compliance or interfere with interpretation of the study
12. Lactating women are excluded from study participation
13. Has previously received SD-101
14. Medical history of significant hypersensitivity, severe and unresolved immune-mediated reactions, severe infusion-related reactions, or allergic reaction to TLR9 agonists or CPI agents in the judgment of the investigator
15. Patients who were enrolled in the Phase 1 portion of the study will not be eligible for enrollment in Phase 1b

Contacts and Locations

Locations

United States, California

UCLA; Recruiting

Los Angeles, California, United States, 90095

Contact: Naomi Long 310-794-2464 NELong@mednet.ucla.edu

Principal Investigator: Bartosz Chmielowski, MD

Stanford; Recruiting

Stanford, California, United States, 94305

Contact: Phuong Pham 650-725-9810 ppham5@stanford.edu

Principal Investigator: Sunil Reddy, MD

United States, Colorado

University of Colorado; Recruiting

Denver, Colorado, United States, 80045

Contact: Gabriel Casareno 720-848-0655 Gabriel.Casareno@CUAnschutz.edu

Principal Investigator: Theresa Medina, MD

United States, Florida

University of Miami; Recruiting

Miami, Florida, United States, 33136

Contact: Clinical Trials Phone Number 305-243-5302

Principal Investigator: Jose Lutzky, MD

United States, Massachusetts

Massachusetts General Hospital; Recruiting

Boston, Massachusetts, United States, 02114

Contact: Kamaneh Montazeri, MD 617-724-4000 kmontazeri@mgh.harvard.edu

Principal Investigator: Kamaneh Montazeri, MD

United States, New York

Columbia University Medical Center; Recruiting

New York, New York, United States, 10032

Contact: Cancer Clinical Trials Email 212-342-5162 cancerclinicaltrials@cumc.columbia.edu

Principal Investigator: Shaheer Khan, DO

United States, Pennsylvania

Thomas Jefferson University; Recruiting

Philadelphia, Pennsylvania, United States, 19107

Contact: Carolyn Palumbo 215-600-7308 carolyn.palumbo@jefferson.edu

Contact: Marlana Orloff, MD marlana.orloff@jefferson.edu

Principal Investigator: Marlana Orloff, MD

University of Pittsburgh Medical Center; Recruiting

Pittsburgh, Pennsylvania, United States, 15232

Contact: Amy Rose, RN 412-647-8587 kennaj@UPMC.EDU

Principal Investigator: Diwakar Davar, MD

United States, Texas

MD Anderson Cancer Center; Recruiting

Houston, Texas, United States, 77030

Contact: Ginny Honaker, RN 713-962-7404 VLHonaker@mdanderson.org

Principal Investigator: Sapna Patel, MD

United States, Washington

Washington University; Recruiting

Seattle, Washington, United States, 98109

Contact: Quynn Jacobs 206-606-7172 qjacobs@seattlecca.org

Principal Investigator: Shailender Bhatia, MBBS

Sponsors and Collaborators

TriSalus Life Sciences, Inc.

More Information

• Responsible Party: TriSalus Life Sciences, Inc.
• ClinicalTrials.gov Identifier: NCT04935229
• Other Study ID Numbers: TS-PERIO-01
• First Posted: June 22, 2021
• Last Update Posted: January 31, 2023
• Last Verified: January 2023

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by TriSalus Life Sciences, Inc.:

Uveal Melanoma; Liver Metastases; TLR9; SD-101

Additional relevant MeSH terms:

Melanoma; Uveal Neoplasms; Nevi and Melanomas; Uveal Diseases; Neuroendocrine Tumors; Neuroectodermal Tumors; Neoplasms, Germ Cell and Embryonal; Neoplasms by Histologic Type; Neoplasms; Neoplasms, Nerve Tissue; Eye Neoplasms; Neoplasms by Site; Eye Diseases; Nivolumab; Ipilimumab; Antineoplastic Agents, Immunological; Antineoplastic Agents; Immune Checkpoint Inhibitors; Molecular Mechanisms of Pharmacological Action