OAKLAND, Calif. — SonALAsense, a pioneer in the development of non-invasive Sonodynamic Therapy (SDT) using SONALA-001 (aminolevulinic acid HCl) in combination with Insightec’s Exablate 4000 Type-2 ultrasound device today announced the presentation of positive preliminary data from the ongoing Phase 1/2 SDT-201 study in Diffuse Intrinsic Pontine Glioma (DIPG). These results were presented at the November 2023 Society for Neuro-Oncology (SNO) Annual Meeting in Vancouver, Canada. The preliminary data from Study SDT-201 shows signals of clinical activity and no safety concerns.
Study SDT-201 is a dose escalation and expansion study in patients with DIPG. Six (6) patients have been treated to date and dose escalation is ongoing. No dose limiting toxicities (DLTs) have been observed and there have been no serious adverse events. There were no treatment related deaths observed. One international patient discontinued for personal reasons and there was one patient death due to metastasis outside of the treated area.
“The preliminary safety, tumor response and clinical performance data we are seeing has the potential to translate into meaningful benefit for these children and their families,” said Ely Benaim, M.D., SonALAsense’s Chief Medical Officer and Executive Vice President of Development. “Currently, radiotherapy is the primary standard of care and many patients are also prescribed steroids. However, these current interventions have the potential for severe side effects.”
Initial clinical activity observed in the first 5 patients showed partial responses of at least 25% reduction in tumor size in 2 (40%) patients through eight weeks post treatment and stable disease in 2 (40%) patients. Four patients treated have exceeded the median survival of 9-11 months post diagnosis. Patients treated have also maintained or improved their patient performance status.
“We are pleased with the early results and the safety profile of SONALA-001 SDT,” said Hasan R. Syed, M.D., pediatric neurosurgeon at Children’s National Hospital and co-lead in Principal Investigator Roger Packer’s trial. “Sonodynamic therapy is part of a larger trend towards less invasive treatment paradigms in neurosurgery. For families of children with DIPG, this trial offers hope and a chance to potentially alter the course of this aggressive disease.”
“As we continue to learn more about our non-invasive therapy through this study, we are extremely encouraged with this preliminary safety and clinical activity data,” said Mark de Souza, CEO, SonALAsense. “Our team remains committed to the DIPG community by continuing to advance this study which shows promise in enhancing quality of life for these patients.”
DIPGs are rare, aggressive, and deadly brain tumors affecting primarily the pediatric population. Approximately 300 children are diagnosed with DIPGs each year in the US, usually between the ages of 5 and 9. There are no effective treatments available beyond radiation, which provides minimal short-term clinical improvement, at best. DIPGs are not amenable to surgical resection.
Lisa Ward, DIPG/DMG community advocate who lost her son to DIPG, is hopeful that this study will lead to a treatment with a better quality of life. “What these children and families go through is absolutely tragic,” said Ward. “The possibility of providing an incisionless, non-toxic approach with therapeutic benefits for these children, that’s everything.”
About SonALAsense
SonALAsense is a clinical-stage company, developing a proprietary form of sonodynamic therapy (SDT) as a first-in-class, noninvasive drug-device combination to treat recurrent glioblastoma, diffuse intrinsic pontine glioma, and other life-threatening cancers. SDT uses SONALA-001 in combination with MR-guided focused ultrasound to selectively target and kill tumor cells.
SONALA-001 has received Orphan Drug Designation for Malignant Gliomas. SONALA-001 in combination with the INSIGHTEC Exablate 4000 Type-2 ultrasound device has received Fast Track Designation for the treatment of patients with DIPG.
Contact:
Valerie Enes
tel. (408) 497-8568