StoppedTrial terminatedSponsor's reason: Business ReasonsShow 4 more changesShow less
Lead sponsor: Merck Sharp & Dohme LLC to Merck Sharp & Dohme LLC
Final enrollment: 30 participants (planned 70)
Primary and study completion dates changed from estimate of Sep 30, 2026 to Sep 29, 2026
Eligibility criteria expanded, about 23 words
MinorPrimary and study completion pushed from Jul 31, 2026 to Sep 30, 2026v30
Re-verified, no change to tracked fieldsv29
MinorTrial status: Recruiting to Active, Not Recruiting
Site details revised at 8 of 8 sites
v28
MinorPrimary and study completion dates: May 29, 2026 to Jul 31, 2026v27
Show 25 earlier versionsHide 25 earlier versions
MinorStudy sites revised (8)v26
Re-verified, no change to tracked fieldsv25
MinorSite details revised at 1 of 8 sitesv24
6 versionsRe-verified since Sep 1, 2023, no change to tracked fieldsv18-v23
MinorStudy sites: 7 to 8v17
Re-verified, no change to tracked fieldsv16
MinorSite details revised at 1 of 7 sitesv15
3 versionsRe-verified since Mar 8, 2023, no change to tracked fieldsv12-v14
MinorPrimary and study completion dates: Jan 19, 2026 to May 29, 2026
Site details revised at 1 of 7 sites
v11
MinorSite details revised at 1 of 7 sitesv10
MinorSite details revised at 1 of 7 sitesv9
MinorSite details revised at 1 of 7 sitesv8
MinorSite details revised at 1 of 7 sitesv7
MinorSite details revised at 1 of 7 sitesv6
MinorStudy sites: 6 to 7v5
MinorStudy sites: 5 to 6v4
MinorStudy sites: 3 to 5v3
NotableTrial status: Not Yet Recruiting to Recruiting
Study sites: 0 to 3
Start date changed from estimate of Jun 23, 2022 to Jun 16, 2022
v2
Study First Submitted
Stopped: an ongoing trial was terminated, suspended or withdrawn.
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to assess the safety and tolerability and to establish a preliminary recommended Phase 2 dose (RP2D) of MK-1484 administered as monotherapy and in combination with pembrolizumab (MK-3475) in adults with advanced or metastatic solid tumors.