LFA102: CLFA102X2102: A phase I, multicenter, open-label study of LFA102 administered intravenously in patients with prolactin receptor-positive castration-resistant prostate cancer or prolactin receptor-positive metastatic breast cancer

Print this page

LFA102: CLFA102X2102: A phase I, multicenter, open-label study of LFA102 administered intravenously in patients with prolactin receptor-positive castration-resistant prostate cancer or prolactin receptor-positive metastatic breast cancer

Primary objectives
Dose Escalation:
1. To determine the MTD or RP2D of LFA102 as a single agent when administered I.V. to adult patients with prolactin receptor-positive castration
resistant prostate cancer (CRPC) or metastatic breast cancer (MBC)
Dose Expansion:
1. To characterize the safety and tolerability of LFA102, including both acute and chronic toxicities
Secondary objectives
1. To characterize single and multiple dose PK of LFA102
2. Prostate cancer: To assess preliminary anti-tumor activity of
LFA102 as a single agent when administered IV to adult patients with prolactin receptor-positive CRPC
3.Breast cancer: To assess preliminary anti-tumor activity of LFA102 as a single agent when administered I.V to adult patients with PRLR-positive MBC
4. To assess any emergence of anti-LFA102 antibodies

Protocol Number051102
Principal InvestigatorMark Stein
PhasePhase I
ScopeNational
Applicable Disease SitesBreast - Female
Prostate
Therapies InvolvedChemotherapy (NOS)
Drugs InvolvedLFA102
Participating InstitutionsRobert Wood Johnson University Hospital in New Brunswick
The Cancer Institute of New Jersey

For further information on this clinical trial, please contact us at 732-235-8675 or cinjclinicaltrials@umdnj.edu.