A Study to Investigate Ubamatamab With and Without REGN7075 in Adult Participants With Advanced/Metastatic Non-Small Cell Lung Cancer (NSCLC)

NCT ID: NCT07154290

Last Updated: 2025-09-04

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 300 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-01-26
• Study Completion Date: 2030-05-17

Brief Summary

This study will evaluate two study drugs called ubamatamab and REGN7075, to see if they can help treat advanced or metastatic Non-Small Cell Lung Cancer (NSCLC), and sarilumab, to evaluate to see if it can help with immune-related side effects from ubamatamab.

The study is looking at:

• How well ubamatamab and REGN7075 works
• The side effects that ubamatamab and REGN7075 might cause
• How much ubamatamab and REGN7075 is in the blood at different times
• If the body makes antibodies to ubamatamab and/or REGN7075, this may cause the ubamatamab to not work as well

Conditions

Advanced/Metastatic Non-Small Cell Lung Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm 1A

Group Type: EXPERIMENTAL

Ubamatamab

Intervention Type: DRUG

Administered per the protocol

Sarilumab

Intervention Type: DRUG

Administered per the protocol

Arm 1B

Group Type: EXPERIMENTAL

Ubamatamab

Intervention Type: DRUG

Administered per the protocol

REGN7075

Intervention Type: DRUG

Administered per the protocol

Sarilumab

Intervention Type: DRUG

Administered per the protocol

Arm 1C

Group Type: EXPERIMENTAL

Ubamatamab

Intervention Type: DRUG

Administered per the protocol

REGN7075

Intervention Type: DRUG

Administered per the protocol

Sarilumab

Intervention Type: DRUG

Administered per the protocol

Arm 2A

Group Type: EXPERIMENTAL

Ubamatamab

Intervention Type: DRUG

Administered per the protocol

Sarilumab

Intervention Type: DRUG

Administered per the protocol

Arm 2B

Group Type: EXPERIMENTAL

Ubamatamab

Intervention Type: DRUG

Administered per the protocol

REGN7075

Intervention Type: DRUG

Administered per the protocol

Sarilumab

Intervention Type: DRUG

Administered per the protocol

Arm 2C

Group Type: EXPERIMENTAL

Ubamatamab

Intervention Type: DRUG

Administered per the protocol

REGN7075

Intervention Type: DRUG

Administered per the protocol

Sarilumab

Intervention Type: DRUG

Administered per the protocol

Interventions

Ubamatamab

Administered per the protocol

Intervention Type: DRUG

REGN7075

Administered per the protocol

Intervention Type: DRUG

Sarilumab

Administered per the protocol

Intervention Type: DRUG

Other Intervention Names

REGN4018; REGN88SAR153191

Eligibility Criteria

Inclusion Criteria

1. Has histologically or cytologically confirmed diagnosis of advanced (stage IIIB not amenable to definitive chemoradiotherapy or stage IIIC) or metastatic (stage IV) NSCLC

2. Has received appropriate first line standard of care treatment for advanced or metastatic NSCLC, as described in the protocol

3. If platinum doublet chemotherapy was not administered as first line therapy, it is required in a later line of therapy prior to enrollment unless there is a documented reason why it is not appropriate

4. Has tumor tissue (archival or fresh) available for testing MUC16 expression by immunohistochemistry inclusion (IHC), as described in the protocol

5. Has at least 1 radiographically measurable lesion by Computed Tomography (CT) or Magnetic Resonance Imaging (MRI) per RECIST v1.1 criteria. Target lesions may be located in a previously irradiated field if there is documented (radiographic) disease progression in that site

6. Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

Exclusion Criteria

1. Has progression of disease fewer than 84 days from starting initial anti-Programmed Cell Death (PD)-(L) 1 therapy

2. Experienced toxicity related to prior treatment that has not resolved to grade 1 prior to initiation of study intervention (except alopecia, hearing loss, grade 2 neuropathy, or endocrinopathy managed with hormone replacement therapy)

3. Has untreated or active primary brain tumor, Central Nervous System (CNS) metastases, leptomeningeal disease, or spinal cord compression, as described in the protocol

4. Current participation OR past participation in another investigational study in which an investigational intervention (eg, drug, vaccine, invasive device) was administered within 4 weeks before planned first dose of study intervention in this clinical study

5. Has received prior monoclonal antibody against PD-(L)1 within 21 days of the first dose of study intervention

6. Has had other prior anti-cancer immunotherapy within 21 days prior to study intervention, as described in the protocol

7. Has received prior cytotoxic chemotherapy within 21 days of the first dose of study intervention

8. Has received an anti-EGFR antibody therapy within the following drug-specific window prior to first dose of study intervention (approximately 5 half-lives), as described in the protocol

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Regeneron Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Clinical Trial Management

Role: STUDY_DIRECTOR

Regeneron Pharmaceuticals

Central Contacts

Clinical Trials Administrator

Role: CONTACT

clinicaltrials@regeneron.com

844-734-6643

Other Identifiers

R4018-ONC-2476

Identifier Type: -

Identifier Source: org_study_id