Publication & Citation Trends
Most Cited Works
Publications
12 total
255TiP AIPAC-003: A randomized, double-blind, placebo-controlled phase III trial testing eftilagimod alpha (soluble LAG-3) in HER2-neg/low metastatic breast cancer patients receiving paclitaxel, following an open-label dose optimization OA
Cited by 1
Semantic Scholar
AIPAC-003: A randomized, double-blind, placebo-controlled phase 3 trial testing eftilagimod alpha (soluble LAG-3) in patients with HER2-neg/low metastatic breast cancer receiving paclitaxel, following an open-label dose optimization.
Cited by 2
Semantic Scholar
Final results from TACTI-002 Part C: A phase II study of eftilagimod alpha (soluble LAG-3 protein) and pembrolizumab in patients with metastatic 2nd line head and neck squamous cell carcinoma unselected for PD-L1.
Cited by 13
Semantic Scholar
11MO Final data from a phase II study (TACTI-002) of eftilagimod alpha (soluble LAG-3) and pembrolizumab in 2nd-line metastatic NSCLC pts resistant to PD-1/PD-L1 inhibitors OA
Cited by 10
Semantic Scholar
675 TACTI-003: A randomized phase IIb study of eftilagimod alpha (soluble LAG-3 protein) and pembrolizumab as first-line treatment of patients with recurrent or metastatic head and neck squamous cell carcinoma OA
Cited by 1
Semantic Scholar
EP08.01-109 TACTI-002: A Phase II Study of Eftilagimod Alpha (Soluble LAG-3) & Pembrolizumab in 2nd line PD-1/PD-L1 Refractory Metastatic NSCLC OA
Cited by 3
Semantic Scholar
1470 Combining the antigen-presenting cell activator eftilagimod alpha (soluble LAG-3) and pembrolizumab: efficacy results from the 1st line non-small cell lung cancer cohort of TACTI-002 (Phase II) OA
Cited by 3
Semantic Scholar
11P Results of a phase II study investigating eftilagimod alpha (soluble LAG-3 protein) and pembrolizumab in second-line PD-1/PD-L1 refractory metastatic non-small cell lung carcinoma pts OA
Cited by 3
Semantic Scholar
Research Topics
CAR-T cell therapy research
(5)
T-cell and B-cell Immunology
(4)
Cancer Immunotherapy and Biomarkers
(4)
Immune Cell Function and Interaction
(4)
Hematopoietic Stem Cell Transplantation
(3)
Frequent Co-Authors
Affiliations
Inserm
Institut Gustave Roussy