Development stage
* RELATED INFORMATION
http://www.clinicaltrials.gov/ct2/show/NCT01387347?term=thymosin+beta+4&rank=6
https://www.clinicaltrials.gov/ct2/show/NCT01393132?term=thymosin+beta+4&rank=7
https://www.clinicaltrials.gov/ct2/show/NCT02597803?term=thymosin+beta+4&rank=9
https://www.clinicaltrials.gov/study/NCT02974907?term=arise-2&rank=4
https://www.clinicaltrials.gov/study/NCT03937882?term=arise-3&rank=1
- ReGenTree has contracted with Ora, Inc., a CRO and SMO company specializing in ophthalmological diseases in the US, to conduct clinical trials to develop the treatment for Dry Eye Disease. The clinical trial uses the CAESM (Controlled Adverse Environment) model to create a more uniform patient response with moderate to severe dry eye. The CAESM Model standardizes influential factors (e.g. relative humidity, temperature and visual tasking) that exacerbate dry eye disease resulting in reduced endpoint variability and improved likelihood of trial success. The CAESM model also allows for rapid data acquisition.
- Completed a Phase IIb/III clinical trial(ARISE-1) of RGN-259 for the treatment of Dry Eye Disease in the US
- Completed a 2nd Phase III clinical trial(ARISE-2) of RGN-259 for treatment of Dry Eye Disease in the US
- Completed a 3rd Phase III clinical trial(ARISE-3) of RGN-259 for the treatment of Dry Eye Disease in the US
- Planning a 4th Phase III clinical trial(ARISE-4) of RGN-259 for the treatment of Dry Eye Disease in the US
Market territory
- ReGenTree has exclusive rights for the development and commercialization of RGN-259 in Worldwide (other than China, Hong Kong, Taiwan).
Please contact HLB Therapeutics if you are interested in partnering (other than China, Hong Kong, Taiwan).