Small Cell Lung Cancer (SCLC) Clinical Trials

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MATCHES-Novel: MAking Telehealth Delivery of Cancer Care at Home Effective and Safe for Novel Therapies: A Hospital-at-Home Model for Tarlatamab Delivery

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to find out whether a Hospital-at-Home (HaH) program is a more efficient way to monitor people's health after receiving tarlatamab than monitoring in the hospital (inpatient).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

∙ Patient

• Diagnosis of extensive stage small cell lung carcinoma (ES-SCLC)

• Treatment plan of commercially available tarlatamab monotherapy as standard of care

• Patients must be 18 years of age or older

• Eastern Cooperative Oncology Group (ECOG) performance status \<2

• Patients must have adequate organ and bone marrow function, defined by the following laboratory results obtained within 28 days prior to the first study treatment:

‣ ANC ≥ 1000 cells/μL (without granulocyte colony stimulating factor support within 4 weeks prior to Cycle 1, Day 1)

⁃ Platelet count ≥50,000/μL (without transfusion within 4 weeks prior to Cycle 1, Day 1)

⁃ Hemoglobin ≥8.0 g/dL (without transfusion within 4 weeks prior to Cycle 1, Day 1)

⁃ Alanine aminotransferase (ALT), aspartate aminotransferase (AST) ≤ 3 X upper limit of normal (ULN). Serum bilirubin ≤ 1.5 x ULN. Patients with known Gilbert disease who have serum bilirubin level ≤ 2 x ULN may be enrolled.

⁃ Estimated Glomerular Filtration Rate (eGFR) ≥ 30mL/min using the CKD-EPI formula.

• The patient is willing to give and sign informed consent

• Appropriate homebound setting as defined by one of the following:

‣ Lodging at MSK Residence or hotel

⁃ 5 New York City boroughs, lower Westchester County (northern boundary Cross County Parkway) and Nassau County (eastern boundary Wantagh State Parkway). This is based on the community paramedic (SeniorCare) 60-minute response time catchment area. If there is any uncertainty about patient residence eligibility, the Principal Investigator will decide after discussion with SeniorCare.

• Patients must be accompanied by a caregiver for the period of time the patient is enrolled in the HaH intervention. For cases where there is uncertainty, the Principal Investigator will make the final determination.

∙ Caregiver

• Primary caregiver as identified by patient enrolled on study

∙ Physician

• Treating physician for patient(s) enrolled on study; managing treatment plan of commercially available tarlatamab as standard of care

Locations
United States
New Jersey
Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities)
RECRUITING
Basking Ridge
Memorial Sloan Kettering Monmouth (Limited Protocol Activities)
RECRUITING
Middletown
Memorial Sloan Kettering Bergen (Limited Protocol Activities)
RECRUITING
Montvale
New York
Memorial Sloan Kettering Suffolk- Commack (Limited Protocol Activities)
RECRUITING
Commack
Memorial Sloan Kettering Westchester (Limited Protocol Activities)
RECRUITING
Harrison
Memorial Sloan Kettering Cancer Center (All Protocol Activites)
RECRUITING
New York
Memorial Sloan Kettering Nassau (Limited Protocol Activities)
RECRUITING
Uniondale
Contact Information
Primary
Robert Daly, MD, MBA
dalyr1@mskcc.org
646-608-3789
Backup
Michael Offin, MD
offinm@mskcc.org
646-608-3763
Time Frame
Start Date: 2025-04-23
Estimated Completion Date: 2028-04-23
Participants
Target number of participants: 70
Treatments
No_intervention: Control Arm
Participants randomized to the control group will receive tarlatamab administration as per usual care.
Experimental: Hospital-at-Home/HAH Intervention Arm
Participants randomized to the intervention group will receive tarlatamab administration through the hospital-at-home care delivery model.
Sponsors
Leads: Memorial Sloan Kettering Cancer Center

This content was sourced from clinicaltrials.gov