House Research Institute Recruiting Patients for Clinical Trial of Medication to Treat NF2 Tumors

Newswise — Los Angeles, Calif. – February 12, 2013 – House Research Institute (HRI) is recruiting patients for a Phase II clinical trial to test a medication that may slow the progression of Neurofibromatosis Type-2, commonly referred to as NF2.

NF2 is a genetic disease characterized by noncancerous tumors in the central nervous system. The disease occurs in 1 in 25,000 births in the United States. A diagnosis of NF2 is made when tumors, called vestibular schwannomas or acoustic neuromas, are found on both auditory nerves. The growth of the tumors can lead to hearing loss, facial paralysis and balance difficulties because the tumors are located on the auditory, balance, and facial nerves. When the tumors are surgically removed, patients are often left completely deaf.

“With few treatment options available other than surgery for patients with NF2, we often watch the tumors and wait as long as possible before operating. Although surgery removes the tumor, we often have to cut the patient’s auditory nerve leaving the patient deaf in that ear,” said Derald Brackmann, M.D., House Clinic Associate and Co-Investigator.

The clinical trial is investigating the medication RAD001 (everolimus), an analog of Rapamycin, to see if the drug is effective in slowing the growth of the vestibular schwannomas in NF2 patients. The pre-clinical research results are promising.

“It was an exciting moment when we first saw the potential effect of this drug on NF2 tumors in our preclinical NF2 mouse model. It is a good candidate for clinical trials in humans,” said Marco Giovannini, M.D., Ph.D., House Research Institute Principal Investigator.

To be eligible to participate in the study, patients must have at least one vestibular schwannoma, which has shown growth in the prior 12 month time period. Patients must also be between 16 and 65 years-old. Up to 25 patients will be enrolled in the clinical trial.

“It is a privilege to work with world leaders in the NF2 field to bring this molecular targeted therapy to patients,” said Joni Doherty, M.D., Ph.D., House Research Institute Co-Investigator.

The study consists of taking RAD001 orally for 12 months or until the tumor shows growth. Tumor growth will be monitored with several MRI scans throughout the 12 months of the study.

In addition to the primary objective of the trial, the secondary objective is to see if RAD001 slows the growth of other central nervous system tumors the patients may have and to see if the patients experience any changes in their hearing.

For more information on the clinical trial, please visit

Support for this House Research Institute clinical trial is provided by Novartis Pharmaceuticals Corp., the manufacturer of the Rapamycin analog RAD001 used for this study, Advocure NF2, and by a grant from the Department of Defense.

Collaborators in this study are Michel Kalamarides, M.D., Ph.D. of Hopital Beaujon, Paris, France; Tena Rosser, M.D. of Children’s Hospital Los Angeles; Naveed Wagle, M.D., USC Norris Cancer Center, Los Angeles; Eva Dombi, M.D. and Brigitte Widemann, M.D., Pediatric Oncology Branch, National Cancer Institute, Bethesda, M.D.

About House Research InstituteHouse Research Institute, formerly House Ear Institute, is a nonprofit 501(c)(3) organization dedicated to improving the quality of life for people with hearing loss and related disorders through scientific research, patient care, and the sharing of knowledge. Institute scientists research the auditory system, at the level of function, as well as at the cellular, molecular and genetic levels. We also explore the neurological interactions between the auditory system and brain, and study ways to improve auditory implants, diagnostics, clinical treatments and intervention methods. We share our knowledge with the scientific and medical communities as well as the general public through our education and outreach programs. For more information about House Research Institute, please call (800) 388-8612 or (213) 483-4431, E-mail [email protected] or visit