Ignite Creation Date:
2024-10-26 @ 3:35 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06517485
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-07-18
Brief Title:
First-in-Human Dose Expansion Study of XMT-1536 in Cancers Likely to Express NaPi2b
Sponsor:
None
Organization:
None
Study Overview
Official Title:
A Phase 1b2 First-in-Human Dose Expansion Study of XMT-1536 In Patients With Solid Tumors Likely to Express NaPi2b
Status:
COMPLETED
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
First-in-human Phase 1b2 safety study of the antibody-drug conjugate ADC XMT-1536 upifitamab rilsodotin administered as an intravenous infusion once every four weeks Patients with platinum-resistant ovarian cancer and non-small cell lung cancer adenocarcinoma subtype were enrolled in the expansion segment of this study In addition to safety assessments the pharmacokinetics of the drug were assessed along with ADC activity
Detailed Description:
This is a multi-center study of XMT-1536 upifitamab rilsodotin in patients with tumors likely to express NaPi2b focusing on patients with platinum-resistant ovarian cancer and non-small cell lung cancer adenocarcinoma subtype XMT-1536 upifitamab rilsodotin was administered as an intravenous infusion once every four weeks Enrollment into the EXP segment consisted of 2 parallel cohorts of patients to confirm the dose that was identified in DES and estimate the objective response rate in each patient population All adverse events were graded according to the National Cancer Institute NCI Common Terminology Criteria version CTCAE v50 Throughout the study pharmacokinetics were measured using proprietary assays developed by Mersana Anti-cancer activity were measured via RECIST
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None