Primary and study completion moved earlier from Mar 2029 to Mar 2028
Eligibility criteria expanded, about 11 words
Site details revised at 52 of 52 sites
MinorStudy sites revised (52)v23
MinorStudy sites revised (52)v22
MinorSite details revised at 1 of 52 sitesv21
MinorSite details revised at 1 of 52 sitesv20
Show 18 earlier versionsHide 18 earlier versions
MinorEnrollment target: 570 to 630v19
MinorSite details revised at 3 of 52 sitesv18
MinorSite details revised at 1 of 52 sitesv17
MinorSite details revised at 1 of 52 sitesv16
MinorSite details revised at 6 of 52 sitesv15
MinorSite details revised at 3 of 52 sitesv14
MinorSite contacts updated at 52 of 52 sitesv13
MinorEnrollment target: 540 to 570
Site contacts updated at 52 of 52 sites
v12
MinorStudy sites: 48 to 52v11
MinorStudy sites: 46 to 48v10
MinorEnrollment target: 530 to 540
Study sites: 45 to 46
Study arms: 2 to 3
Study title expanded, about 1 word
v9
Re-verified, no change to tracked fieldsv8
MinorStudy sites: 43 to 45v7
MinorStudy sites: 8 to 43v6
MinorStudy sites: 5 to 8v5
MinorStudy sites: 41 to 5
Collaborators shortened, about 3 words
v4
MinorStudy sites: 2 to 41v3
NotableTrial status: Not Yet Recruiting to Recruitingv2Show 4 more changesShow less
Study sites: 0 to 2
Primary and study completion dates: Mar 31, 2029 to Mar 2029
Start date changed from estimate of Sep 15, 2024 to Sep 12, 2024
Eligibility criteria expanded, about 1 word
Study First Submitted
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 main purpose of this study is to assess safety \& tolerability and antitumor activity of LY3962673 as monotherapy and in combination with other chemotherapy agents in participants with KRAS G12D-mutant advanced solid tumor types. The study is expected to last approximately 5 years.