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Asia

Avecho to Continue With Full Enrollment in Insomnia Trial After Positive Data Monitoring Board Recommendation; Shares Hit 5.5-Year High

Avecho Biotechnology (ASX:AVE) said an independent data monitoring board recommended that the company's phase 3 clinical trial evaluating TPM-enhanced cannabidiol capsule for insomnia continue to the full planned enrolment of 519 participants, according to a Wednesday filing with the Australian bourse.The data monitoring board issued the recommendation following an interim analysis that showed no serious adverse events across 244 initial participants."The interim analysis represents a major value-inflection point for the program, reducing clinical development risk and providing a defined pathway toward completion of the pivotal study," the company said.Avecho added that it has already identified additional clinical sites to speed up the recruitment of the second patient cohort.The company's shares gained 33% in recent Wednesday activity and earlier hit their highest since December 2020.

ASX:AVE
Asia

Avecho Biotechnology Receives AU$1.98 Million Under Australian R&D Tax Incentive Scheme

Avecho Biotechnology (ASX:AVE) said it has received AU$1.98 million for the year ended Dec. 31, 2025, under the Australian Government's research and development tax incentive scheme, according to a Friday Australian bourse filing.The company said AU$1.62 million of the funds will be used to repay Endpoint Capital for advances on the company's R&D tax credit paid over the past year, with the remainder to support operations and advance its commercialization strategy.

ASX:AVE
Asia

Avecho Biotechnology Completes Treatment Phase for Interim Analysis of Third-Phase Insomnia Trial

Avecho Biotechnology (ASX:AVE) completed the treatment phase for the last patient required for the planned interim analysis of its pivotal third-phase insomnia trial evaluating its tocopheryl phosphate mixture-enhanced cannabidiol capsule, according to a Thursday filing with the Australian bourse.The analysis is expected to provide the first indication of the product's efficacy profile, determine the number of participants needed for the final study, and support ongoing licensing discussions, the filing said.Results are expected in late June, per the filing.

ASX:AVE

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