Phase 1 Trial of LVGN6051 as Single Agent and in Combination With Keytruda (Pembrolizumab) in Advanced or Metastatic Malignancy

Cancer Clinical Trial

Official title:

An Open Label, First in Human (FIH), Phase 1 Trial of LVGN6051 as Single Agent and in Combination With Keytruda (Pembrolizumab) in Advanced or Metastatic Malignancy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04130542
• Other study ID #: LVGN6051-101
• Secondary ID: MK-3475-A31/KEYN
• Status: Recruiting
• Phase: Phase 1
• Start date: October 31, 2019
• Est. completion date: December 2024

Study information

• Verified date: January 2024
• Source: Lyvgen Biopharma Holdings Limited
• Contact: Lynn Jiang, PhD
• Phone: 1-484-686-9652
• Email: lynn.jiang[@]lyvgen.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

LVGN6051 is a humanized monoclonal antibody that specifically binds to CD137, and acts as an agonist against CD137.

This first in human study of LVGN6051 is designed to establish the maximum tolerated dose (MTD) and/or the recommended dose for expansion (RDE) as well as the recommended Phase 2 dose(s) (RP2D) of LVGN6051, both as a single agent (monotherapy) and in combination with a fixed dose of anti-PD-1 antibody (Pembrolizumab/MK-3475) in the treatment of advanced or metastatic malignancy.

Description:

This is an open-label, non-randomized, two-stage, FIH Phase 1 study, utilizing an accelerated dose escalation followed by a traditional 3 + 3 dose escalation algorithm to identify the MTD and/or RDE and RP2D of LVGN6051 as a single agent (monotherapy) and in combination with pembrolizumab (MK-3475). The first stage of the study is the dose escalation phase (i.e., Phase 1a). The second stage of the study is the dose expansion phase (i.e., Phase 1b). During the study, dose interruption(s) and/or delay(s) may be implemented based on toxicity. Dose modifications are not permitted. Intra-patient dose escalations will be allowed for the early dose cohorts (single-patient dose groups) in Phase 1a Part 1. Patients will be considered evaluable for safety and tolerability if they receive at least one dose of LVGN6051 or pembrolizumab (MK-3475) at the specified cohort dose. Patients in all parts of the trial will remain on therapy until confirmed disease progression or for 2 years, whichever occurs first. However, patients who are clinically unstable will discontinue following the initial assessment of disease progression.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 276
• Est. completion date: December 2024
• Est. primary completion date: October 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Males or females aged = 18 years.

• Ability to understand and willingness to sign a written informed consent document.

• Patients must have a histologically or cytologically confirmed metastatic or unresectable malignancy.

• Estimated life expectancy, in the judgment of the Investigator, of at least 90 days.

• Adequate bone marrow, liver, and renal functions.

• Men and women of childbearing potential must agree to take highly effective contraceptive methods.

• Patients should recover from all reversible AEs of previous anticancer therapies to baseline.

• Patients infected with the HIV virus will be eligible if the disease is under control of effective therapy.

Exclusion Criteria:

• Receipt of systemic anticancer therapy including investigational agents or devices within 5 half-lives of the first dose of study treatment.

• Previous radiotherapy within 14 days of the first dose of study treatment.

• Known active CNS metastasis and/or carcinomatous meningitis.

• Has received a live-virus vaccine within 30 days.

• Has had a Grade = 3 allergic reaction to treatment with a monoclonal antibody.

• Abnormality of QT interval or syndrome.

• Patients with history of Grade = 3 immune-related AEs (irAEs) or irAE.

• Patients who are receiving an immunologically-based treatment for any reason.

• Treatment with systemic immune-stimulatory agents within 4 weeks prior to the first dose of study drug.

• Active or chronic autoimmune disease that has required systemic treatment in the past 2 years or who are receiving systemic therapy for an autoimmune or inflammatory disease.

• Has a clinically significant cardiac condition, including unstable angina, acute myocardial infarction within 6 months.

• Has an active infection requiring intravenous (i.v.) anti-infectives within 14 days before the first dose of study treatment.

• Current evidence or history of interstitial lung disease or active, noninfectious pneumonitis requiring treatment such as oral or intravenous glucocorticoids to assist with management.

• Female patients who are pregnant or breastfeeding.

• Any evidence of severe or uncontrolled systemic disease.

• Any other disease or clinically significant abnormality in laboratory parameters.

• Has previously had a stem cell or bone marrow or solid organ transplant.

Related Conditions & MeSH terms

• Cancer
• Neoplasms

Intervention

Biological:
• LVGN6051
IV infusion once every 3 weeks (Q3W).
• KEYTRUDA® (pembrolizumab)
IV infusion once every 3 weeks (Q3W).

Locations

Country	Name	City	State
United States	The Johns Hopkins University	Baltimore	Maryland
United States	MD Anderson Cancer Center	Houston	Texas
United States	Verdi Oncology Research	Lafayette	Indiana
United States	NYU Langone Health	New York	New York
United States	Nebraska Cancer Specialist	Omaha	Nebraska
United States	University of California Irvine Health	Orange	California
United States	UCSF Helen Diller Family Comprehensive Cancer Center	San Francisco	California

Sponsors (2)

Lead Sponsor	Collaborator
Lyvgen Biopharma Holdings Limited	Merck Sharp & Dohme LLC

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety/Tolerability	mEvaluate the safety and tolerability and determine the Maximum tolerated dose (MTD) and/or recommended dose for expansion (RDE) and recommended Phase 2 dose(s) (RP2D) of LVGN6051 administered as a single agent (monotherapy) and in combination with pembrolizumab, in adult patients with advanced malignancy.	up to 24 months