Starting Wednesday, October 15, 2025, join us monthly on Wednesdays from 2:30-3:30PM in Galapagos (75A-5-5001) at Broad and online at broad.io/L2CAM to share ideas and data with other investigators working on rare disease projects.

The L2C Accelerator meeting is open to scientists of all backgrounds including physician-scientists, students, and postdocs with a Broad ID.

Organizers/co-chairs: Michelle Rengarajan, Sarah Morton, Sumaiya Iqbal, Vijay Sankaran, Matt Sampson, and Jillian Shaw.

***

10/15/25 Speaker(s): Masha Alimova, Oivin Guicherit, Ranjith Muraleedharan
Optical Screening Technologies and Approaches for Drug Discovery in Rare Diseases

11/12/25 Speaker(s): Brad Wertheim and George Alba
VEGF as a targetable node for pulmonary vascular diseases

12/10/25 Speaker(s): Alfred Pokmeng See
A proposal to develop scalable platforms to identify therapeutics for EPHB4-driven vein of galen malformation

1/7/26 Speaker(s): Michelle Rengarajan
Data-driven framework for optimized ASO selection in Duchenne Muscular Dystrophy

2/4/26 Speaker(s): Matt Goddeeris
L2C: Every Cure

3/11/26 Speaker(s): Sami Farhi and Lindsey Erion Barner
L2C: STP Platform Capabilities

4/1/26 Speaker(s): Steve Carr and Namrata Udeshi
L2C: Proteomics

4/15/26 Speaker(s): Runxi Shen, Maria Lozada, Beth Cimini
Systematic rare disease phenotype and drug discovery - advances in imaging