A clinical trial evaluating IMX-110 in pediatric patients with rhabdomyosarcoma
Latest Information Update: 16 Jun 2023
At a glance
- Drugs IMX-110 (Primary)
- Indications Rhabdomyosarcoma
- Focus Adverse reactions
- 14 Jun 2023 According to an Immix Media Release, the company announced that it has completed its previously announced at-the market equity offering program. It has completed 5 million dollars common stock offering. It intends to use net proceeds from the ATM offering for its IMX-110 plus tislelizumab phase 1b combination clinical trial, its IMX-110 monotherapy clinical trial and general corporate purposes.
- 21 Nov 2022 New trial record
- 11 Nov 2022 According to Immix Biopharma media release, company has received Institutional Review Board (IRB) approval to enroll pediatric patients in this trial. Enrolling pediatric patients in a clinical trial is a key requirement for FDA approval of a Priority Review Voucher.