B&K Corporation Limited (B&K) disclosed that patient enrollment for the Phase II clinical trial of its recombinant human platelet-derived growth factor BB (rhPDGF-BB) gel, Pro-101-2, has been completed.
The randomized, double-blind, placebo-controlled study is designed to evaluate the efficacy and safety of Pro-101-2 in treating diabetic foot ulcers and to collect key parameters for a planned Phase III trial.
Management highlighted the milestone as a significant step in the company’s diabetic foot ulcer research program.
In accordance with Rule 18A.05 of the Hong Kong Listing Rules, B&K emphasized that there is no assurance Pro-101-2 will ultimately obtain regulatory approval or reach the market. Shareholders and potential investors are advised to exercise caution when dealing in the company’s shares.
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