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RONA THERAPEUTICS is a pioneering nucleic acid therapeutics company to discover, develop and deliver transformative modular RNA medicines to treat patients globally.
LEARN MORERona Therapeutics is a world-leading nucleic acid therapeutics company dedicated to addressing metabolic and degenerative diseases.
Since its inception in 2021, Rona Therapeutics has advanced several potential best-in-class siRNA therapeutics in the clinic. With longer duration, deep knockdown and improved tolerability, Rona Therapeutics' metabolic assets have demonstrated a differentiated profile to address unmet needs in cardiovascular diseases, MASH and obesity.
The company has built a proprietary extrahepatic delivery platform in obesity and neurodegenerative diseases to fully exploit nucleic acid delivery potential beyond the liver. With robust knockdown potency and long-term duration (Q9M or longer), multiple assets are progressing into IND-enabling stage to treat complex diseases that cannot be treated with conventional modalities.
~$200M USD
Raised from global leading long-only funds and strategic partners
Leadership with deep expertise in biopharma, venture capital, and translational research
Chief Executive Officer
Founder with ~15 years of biopharmaceutical and venture capital experience, previously Managing Director at Lilly Asia Ventures.
Chief Medical Officer
Executive Vice President of Translational Research, joined in January 2025.
SVP of Chemistry
Senior leader in nucleic acid chemistry and drug development.
EVP of Discovery & Research
Driving innovation in RNA discovery and preclinical development.
VP of CMC
Expertise in chemistry, manufacturing, and controls for RNA therapeutics.
VP of Finance & Corp Dev
Led $200M+ in funding rounds and strategic partnerships.
Next-generation delivery systems enabling durable, targeted, and safe RNA therapeutics
Long dosing intervals to improve patient compliance
Convenient subcutaneous injection
Novel GalNAc and chemical modifications for improved potency and safety
Small molecule conjugation for efficient receptor-mediated uptake in CNS
Intrathecal local delivery to minimize systemic side effects
Q6M or longer dosing with proof-of-concept in non-human primates
Ideal for complex diseases like cardiovascular disorders and obesity
Potential to treat multiple diseases via dual-targeting
Synergistic efficacy without added side effects; streamlined development
Innovative siRNA therapeutics targeting high-unmet medical needs
Hypertriglyceridemia | ApoC3
Long-acting APOC3-targeting siRNA. Presented Phase 1 data at AHA 2025. FDA IND approved for Phase 2 (Mar 2025).
Obesity | INHBE
Highly potent and durable INHBE siRNA. IND filed (Sep 2025). Targets obesity with long-acting mechanism.
ASCVD | PCSK9-Lp(a)
Dual-targeting siRNA for atherosclerotic cardiovascular disease. Early preclinical development.
PCSK9 siRNA
Innovative PCSK9 siRNA. First subject dosed in Australia (Aug 2023), IND approved in China (Dec 2023).
Hypertension | AGT
Novel angiotensinogen (AGT)-targeting siRNA. NMPA IND approved for Phase 1 (Apr 2025).
Neurodegenerative Disease
Utilizing APOLLO platform for CNS delivery. Early-stage discovery.
MASH | Multi-Target
Bi-valent siRNA targeting metabolic dysfunction in MASH. Preclinical optimization.
Kidney Disease | Glomerulonephritis
Co-developed with Keymed. First-in-class siRNA for severe kidney diseases.
October 11, 2025 — Data demonstrates significant ApoC3 knockdown and triglyceride reduction with favorable safety profile.
September 15, 2025 — Highly potent INHBE siRNA enters regulatory review for Phase 1 clinical trials.
April 21, 2025 — Novel AGT-targeting siRNA approved to begin Phase 1 trials in China.
For business development, recruitment, and partnership inquiries
Tower 3, JNB Life Science Park, No.795, Kangwei Road, Pudong New Area, Shanghai, China
BD@ronatherapeutics.com
HR@ronatherapeutics.com
SE 2 202-220 FERNTREE GULLY RD, CLAYTON VIC 3168
BD@ronatherapeutics.com
State of Delaware
BD@ronatherapeutics.com
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