LAM Pilot Study with Imatinib LAMP-2
Abstract
This pilot trial employs a dual agent design intended to generate safety and efficacy data sufficient to power and design a longer-term trial of imatinib in the treatment of LAM. The hypothesis is that imatinib can be safely co-administered with sirolimus and will result in change in serum biomarkers of LAM. Durability of response will not be tested. Importantly, the widely established LAM biomarker of disease activity, VEGF-D will be used in this small clinical trial design using 20 participants. The there specific aims are: Specific Aim 1: To determine the safety and tolerability of Imatinib in the treatment of LAM. Specific Aim 2: To determine the safety and tolerability of concurrent imatinib and sirolimus treatment in LAM. Specific Aim 3: To evaluate the effect of imatinib treatment on serum biomarkers of LAM.
Document Details
- Document Type
- Technical Report
- Publication Date
- Jul 01, 2023
- Accession Number
- AD1216892
Entities
People
- Jeanine M. D'Armiento
Organizations
- Columbia University