This project has been flagged by a community member as inappropriate due to reason below.*

Expert Interview

Slingshot members are talking to an expert! The topic is:

A Third Look: Discussing the FDA approval of Columvi (glofitamab-gxbm) for patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL)

Ticker(s): RHHBY

Who's the expert?

  • Certified in Internal Medicine and Board Eligible in Hematology and Oncology.
  • Member of the American Society of Clinical Oncology (ASCO) and American Society of Hematology (ASH). He is also a member of the AMA and ACP.

Interview Goal
This call will focus on the data from The Phase I/II NP30179 Study on Columvi, which supported the FDA approval for treatment of DLBCL

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Reason

*Slingshot Insights provides access to information, not investment advice. We work to support you and facilitate access to experts; however we are not responsible for monitoring calls for the disclosure of MNPI. You should obtain financial, legal and tax advice from your qualified and licensed advisers before deciding to invest in any security.