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aTyr Pharma, Inc.

aTyr Pharma, Inc. is a clinical-stage biotechnology company that discovers and develops product candidates translating tRNA synthetase biology into therapies for fibrosis and inflammation in the United States. Its lead candidate, efzofitimod, is a selective NRP2 modulator in a Phase 3 trial for pulmonary sarcoidosis, a Phase 2 trial for sarcoidosis and systemic sclerosis-associated interstitial lung diseases (ILDs), and development for other ILDs such as chronic hypersensitivity pneumonitis (CHP) and connective tissue disease-related ILD. The company is also developing ATYR0101, a fusion protein derived from an aspartyl-tRNA synthetase domain, in preclinical development for fibrosis, and ATYR0750, an alanyl-tRNA synthetase domain, for liver disorders. It has a collaboration and license agreement with Kyorin Pharmaceutical Co., Ltd. for the development and commercialization of efzofitimod for ILDs in Japan. aTyr Pharma, Inc. was incorporated in 2005 and is headquartered in San Diego, California.

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Biotech & Genomic Medicine

aTyr Pharma cuts workforce 60% to advance efzofitimod into Phase 3

aTyr Pharma announced a corporate restructuring that includes a 60% workforce reduction to advance its lead therapeutic candidate efzofitimod in interstitial lung disease. The company's second-quarter 2026 net loss narrowed to $10.31 million, or $0.11 per share, from $19.53 million, or $0.22 per share, a year earlier. Cash and equivalents stood at $58.9 million as of June 30, 2026, which aTyr expects will fund operations into late 2028. The restructuring and additional cost-saving measures are projected to reduce annualized operating expenses by approximately $13 million starting in the fourth quarter of 2026. Chief Financial Officer Jill Broadfoot will step down on September 30, 2026, and Vice President of Finance Brandon Yaras will become CFO on October 1, 2026. The company anticipates FDA feedback on the Phase 3 protocol for efzofitimod in pulmonary sarcoidosis by the end of August 2026, and topline results from the Phase 2 EFZO-CONNECT study in systemic sclerosis-related ILD are expected in the first quarter of 2027.
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