first patients have been dosed in a multi-regional Phase IIB randomized, placebo-controlled clinical trial for the treatment of hepatitis B-associated liver cancer.
Being tested in the first line setting is a first-in-class botanical drug candidate, YIV-906 (also known as PHY906 and KD018), whose development has been supported by the National Foundation for Cancer Research (NFCR) for two
decades. YIV-906 is a proprietary formulation of four herbs.
Patients began enrolling in the United States and Taiwan, with Hong Kong and Mainland China to follow. If, following these and future Phase III trials, the drug is approved by the U.S. Food and Drug Administration (FDA), it would be the country's first authorization for usage of a purely botanical cancer drug and usher in a new paradigm for drug discovery.
YIV-906 is an immune-enhancing and cytoprotective cancer therapeutic candidate which received orphan drug designation by the FDA in 2018 and that in preclinical studies has demonstrated:
enhancement of both the innate and adaptive immune system in the tumor microenvironment--via polarizing M1 macrophanges and activating T-cells--when in combination with immunotherapy, chemotherapy and radiation therapies;
protection of the gastrointestinal tract by reducing inflammation--via IL-6, NF-kappa-B, COX2, and iNOS pathways; and
sped-up tissue regeneration by promoting progenitor and stem cell growth--via the WNT signaling pathway.
It is now being clinically tested in combination with sorafenib, which when administered as a m
onotherapy is often effective but causes dose-limiting side effects that result in one in three patients at least temporarily choosing to discontinue use.
In early-stage Phase I/II trials in liver, pancreatic and colorectal cancers, YIV-906 has demonstrated safety and promising efficacy, with the potential to improve survival and quality of life for patients.
The developer of YIV-906, Yung-Chi Cheng, Ph.D., Henry Bronson Professor of Pharmacology at Yale University, has been an NFCR-funded researcher since 1991. He has discovered or developed four approved small molecule drugs for the treatment of hepatitis B, cytomegalovirus and AIDS.
Dr. Cheng is a pioneer in pharmacology who is applying a systems biology approach to botanical medicines that address complex aging-associated diseases.
He and his laboratory are employing rigorous modern human drug validation principles and bioinformatics to learn from traditional medicines, and mechanism-based quality control to manufacture consistent complex mixtures.
Over the past two decades and with NFCR support, Dr. Cheng has transitioned his focus from small molecule to botanical drug discovery.
By mining human experience of botanical medicines--including traditional Chinese medicines (TCM)--using modern technology and techniques, he has developed the STAR (Signal Transduction, Action and Response) Discovery platform.
Among Dr. Cheng's most intensively reviewed and extensively published research has been that on YIV-906, the proprietary formulation of four herbs which he has been studying since 1999 that is now under clinical review.
The FDA created a new regulatory pathway for botanical drugs in 2004 and updated its Botanical Drug Guidance in 2016, creating new opportunities for botanical therapeutics--provided they demonstrate efficacy, safety and consistent batch-to-batch manufacturing.
Dr. Cheng and Yale Unive
rsity co-founded the company Yiviva to carry out human studies on YIV-906 and other herbal medicine formulas for multiple cancer indications.
It will be recruiting hepatitis B-associated liver cancer patients for twenty clinical sites, include Memorial Sloan Kettering Cancer Center, National Cancer Center of China, Taipei Medical University and Queen Mary Hospital in Hong Kong.