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SHANGHAI, March 2, 2022 /PRNewswire/ -- RedCloud Bio (the "Company"), an innovative biotech company integrating structural pharmacology and computational approaches to advance small molecule drug development, announced today that the US Food and Drug Administration (FDA) has accepted the Company's Investigational New Drug (IND) application, clearing the path to proceed Phase I/IIa clinical investigation of H002, a broad spectrum, highly selective, fourth-generation compound. The candidate will be initially evaluated for treating C797S mutation-driven resistance to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) in non-small cell lung cancer (NSCLC). H002 is the first drug candidate expected to enter clinical trials from RedCloud Bio's pipeline.
"The IND acceptance and anticipated start of our global clinical studies, represent important milestones in our Company's growth and validation of our internally developed small molecule discovery platform," said Mai-Jing Liao, Ph.D., CEO of RedCloud Bio.
H002 was developed with RedCloud Bio's proprietary small molecule drug discovery platform. The platform combines computational approaches, including computational chemistry and artificial intelligence (AI), with structural pharmacology that differentiates interactions between drug candidates and disease-causing mutations of target proteins at an atomic level.
"TKIs can afford an important therapeutic option for NSCLC patients. However, emergence of resistant mutations to successive generations of therapeutics can compromise TKIs' efficacy," noted Dr. Liao. "The C797S mutation, in combination with several other mutations, has emerged as one of the most common mechanisms for on-target resistance to third-generation EGFR TKIs such as osimertinib. These combinations have been found in seven to fifteen percent of third generation TKI-treated NSCLC patients."
H002 has demonstrated potential in overcoming resistance in C797S mutations. The compound has also shown significant inhibitory effects on wide spectrum of single, double and triple EGFR mutants in laboratory studies. High bioavailability and favorable tissue distribution as well as a wide therapeutic window have also been observed in preclinical studies.
Studies have demonstrated that H002 has high selectivity, a wide spectrum and potent anti-tumor activity against various EGFR activating mutations, as well as favorable safety profiles. RedCloud Bio expects to develop H002 as a next-generation EGFR inhibitor, targeting high unmet medical needs in EGFR-mutated NSCLC, including emerging drug resistance to existing EGFR TKI.
About RedCloud Bio
RedCloud Bio is an innovative biotech company integrating novel technologies to advance small molecule drug discovery and development. The Company has laboratories in Shanghai, Beijing and Xiamen with drug discovery platform integrating structural pharmacology, computational chemistry approaches and AI technologies, and with developing global clinical development capabilities.
RedCloud Bio has accumulated structural data and algorithm models covering clinically important targets, and has built an innovative pipeline targeting tumor resistance, rare and other critical diseases with high unmet medical needs, using its core technology platform. The Company's lead therapeutic candidate, H002, is a small molecule compound addressing EGFR activating mutations, and is expected to enter global clinical trials. The compound is a promising candidate as a next-generation TKI with unique clinical differentiation for NSCLC.
For information, contact PR@redcloudbio.com / Tang He, tang.he@redcloudbio.com
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