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InvestorNewsBreaks – Cabaletta Bio Inc. (NASDAQ: CABA) Featured in Mizuho Securities Research Report
August 5, 2021

InvestorNewsBreaks – Cabaletta Bio Inc. (NASDAQ: CABA) Featured in Mizuho Securities Research Report

Cabaletta Bio (NASDAQ: CABA) was featured in a recent equity research report published by Mizuho Securities USA LLC. The report reads, “Cabaletta released 2Q21 earnings that were essentially a non-event, as is often the case for a clinical-stage company. More important are updates on the progress of lead program DSG3-CAART, and we are encouraged by the DesCAARTes trial update that no dose limiting toxicities or clinically relevant adverse events have been observed to date, while we await key target engagement data that the company expects to provide 3 to 6 months after completion of dosing of each cohort. Management also expects to submit an IND for MuSK-CAART in myasthenia gravis, and hold a pre-IND meeting with FDA for their PLA2R-CAART program in membranous nephropathy in 2H21. We maintain our $22 PT, and reiterate our Buy rating.”

To request access to the full report, visit https://ibn.fm/YjeoO

About Cabaletta Bio Inc.

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(TM)) platform, in combination with Cabaletta’s proprietary technology, utilizes Chimeric AutoAntibody 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(TM) 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(TM) Phase 1 clinical trial, please see www.clinicaltrials.gov. 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 the company’s website at www.cabalettabio.com.

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