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Study of RYZ101 in Combination With SoC in Subjects With SSTR+ ES-SCLC

Active, not recruiting · Phase 1 · NCT05595460

Conditions: SCLC,Extensive Stage

At a glance

Research payments reported, 2025
$1.4M
U.S. investigators named
16
Sites paid
15
Planned or actual enrollment
21

About the trial

Sponsor
RayzeBio, Inc.
Tested
RYZ101 Dose Level 1 (drug), RYZ101 Dose Level 2 (drug), RYZ101 Dose Level 3 (drug), RYZ101 Dose Level -1 (drug), Atezolizumab (drug), Carboplatin (drug), Etoposide (drug)
Dates
Started 2022-10-10; completion 2027-07
Results posted
Not yet

This study aims to determine the safety, preliminary antitumor activity, and pharmacokinetics (PK) of RYZ101 in combination with standard of care (SoC) therapy consisting of carboplatin + etoposide + atezolizumab in untreated subjects with somatostatin receptor expressing (SSTR+) ES-SCLC.

From ClinicalTrials.gov, last updated 2026-04-13. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $1.4M in research payments for this study in 2025 (15 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.