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Cabaletta Bio to Participate in Upcoming Investor Conferences in November

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On November 9, 2021, Cabaletta Bio, a clinical-stage biotechnology company focused on engineered T cell therapies for B cell-mediated autoimmune diseases, announced its participation in two investor conferences. The events include the Guggenheim Securities 3rd Annual Neuro/Immunology Conference on November 16 and the Evercore ISI 4th Annual HealthCONx Conference on November 30, featuring fireside chats by CEO Steven Nichtberger. The company’s proprietary CABA™ platform targets specific autoantibody-producing B cells and is evaluating its lead candidate, DSG3-CAART, in a Phase 1 trial.

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PHILADELPHIA, Nov. 09, 2021 (GLOBE NEWSWIRE) -- Cabaletta Bio, Inc. (Nasdaq: CABA), a clinical-stage biotechnology company focused on the discovery and development of engineered T cell therapies for patients with B cell-mediated autoimmune diseases, today announced that the Company will participate in two upcoming investor conferences in November:

  • Guggenheim Securities 3rd Annual Neuro/Immunology Conference: Steven Nichtberger, M.D., President and Chief Executive Officer, will participate in a fireside chat on Tuesday, November 16, 2021 at 8:15 a.m. ET. Members of management will also be available for one-on-one meetings.

  • Evercore ISI 4th Annual HealthCONx Conference: Steven Nichtberger, M.D., President and Chief Executive Officer, will participate in a fireside chat on Tuesday, November 30, 2021 at 12:35 p.m. ET. Members of management will also be available for one-on-one meetings.

Both presentations will be available on the News and Events section of the company’s website at www.cabalettabio.com. Replays will be available on the website for 90 days.

About Cabaletta Bio
Cabaletta Bio is a clinical-stage biotechnology company focused on the discovery and development of engineered T cell therapies, and exploring their potential to provide a deep and durable, perhaps curative, treatment, for patients with B cell-mediated autoimmune diseases. The Cabaletta Approach to selective B cell Ablation (CABA™) platform, in combination with Cabaletta’s proprietary technology, utilizes Chimeric Auto Antibody Receptor (CAAR) T cells that are designed to selectively bind and eliminate only specific autoantibody-producing B cells while sparing normal antibody-producing B cells, which are essential for human health. The Company’s lead product candidate, DSG3-CAART, is being evaluated in the DesCAARTes™ Phase 1 clinical trial as a potential treatment for patients with mucosal pemphigus vulgaris, a prototypical B cell-mediated autoimmune disease. The FDA granted Fast Track Designation for DSG3-CAART in May 2020. For more information about the DesCAARTes™ Phase 1 clinical trial, please visit our website (DesCAARTes™ Phase 1 Trial). The Company’s lead preclinical product candidate, MuSK-CAART, is in IND-enabling studies and is designed as a potential treatment for patients with MuSK-associated myasthenia gravis. For more information, visit www.cabalettabio.com.

Contacts:
Anup Marda
Chief Financial Officer
investors@cabalettabio.com

Sarah McCabe
Stern Investor Relations, Inc.
212-362-1200
sarah.mccabe@sternir.com


FAQ

When will Cabaletta Bio participate in the Guggenheim Securities Conference?

Cabaletta Bio will participate in the Guggenheim Securities 3rd Annual Neuro/Immunology Conference on November 16, 2021, at 8:15 a.m. ET.

What is the focus of Cabaletta Bio's CABA™ platform?

The CABA™ platform focuses on selective B cell ablation, specifically targeting autoantibody-producing B cells involved in autoimmune diseases.

When will the fireside chat at the Evercore ISI HealthCONx Conference take place?

The fireside chat at the Evercore ISI 4th Annual HealthCONx Conference will take place on November 30, 2021, at 12:35 p.m. ET.

What is DSG3-CAART being evaluated for?

DSG3-CAART is being evaluated as a potential treatment for mucosal pemphigus vulgaris in the DesCAARTes™ Phase 1 clinical trial.

Has DSG3-CAART received any designations from the FDA?

Yes, DSG3-CAART received Fast Track Designation from the FDA in May 2020.