CIVATECH ONCOLOGY, INC. — Department of Health and Human Services SBIR Phase I: 102

CIVATECH ONCOLOGY, INC. — SBIR Phase I award from Department of Health and Human Services.

Amount
$299,599
Agency
Department of Health and Human Services · National Institutes of Health
Program / Phase
SBIR · Phase I
Topic
102
Solicitation
PA15-269
NAICS
Place of performance
NC
Period
2016-09-13 → 2017-08-31

Description

CivaTech Oncology s mission is to provide improved radiation therapy directly to localized tumors The Company has developed a novel polymer encapsulated membrane like radiation source that emits radiation on only one side of the device the CivaSheet This directional source is compatible with open and minimally invasive surgical techniques and has FDA clearance to be used as primary or combined cancer therapy The CivaSheet is a partially bio absorbable implant that can be applied at the time of the initial surgery The CivaSheet decreases the time between surgery and radiation therapy which is a benefit to the patient Additionally the CivaSheet can shield healthy tissues while irradiating the diseased tissue or tumor margin This shielding enables the CivaSheet to be implanted close to radiosensitive structures without overdosing them a huge advantage for cancers in the abdomen In Phase I CivaTech Oncology will confirm the CivaSheet does not move after implantation and that excellent dosimetry can be achieved The CivaSheet will be implanted during the Whipple procedure for pancreas resection a standard of care procedure for resectable pancreatic patients The CivaSheet will benefit these patients by delivering radiation therapy at the time of initial surgery to minimize delay in the treatment Pancreatic cancer is an aggressive disease that progresses quickly Faster treatment cycles are ideal for cancer types that proliferate quickly In Phase I the safety of CivaSheet and general recommendations for its use in this patient population will be assessed A Clinical Evaluation Team will review the clinical trial protocols plans for implants sample dosimetry that can be achieved and eventually each patient case to evaluate device related events The Clinical Evaluation Team will agree with Physicians on site to continue treating patients in Phase II The Phase II will consist of two concurrent clinical trials exploring the use of the CivaSheet as monotherapy or boost therapy in resectable pancreatic cancer patients The rate of local recurrence in patients implanted with CivaSheet will be compared to the current rate of Additionally the quality of life pain and mortality in each patient will be monitored CivaSheet will reduce the radiation delivered to adjacent duodenum stomach and liver and should result in fewer side effects Additionally it will provide a conformal dose reduce the risk for infection and possibly reduce treatment related side effects The Clinical Evaluation Team will review each patient case to discuss patient specific differences impacting the device to increase knowledge and benefit future surgical procedures CivaSheet is a truly unique brachytherapy device that has the potential to become the first line of defense for localized cancer CivaTech Oncology is committed to making the CivaSheet available to cancer patients in multiple indications CivaTech Oncology has a membrane like brachytherapy device the CivaSheet that is truly customizable to a specific patientandapos s condition and offers a unidirectional option to shield healthy tissue Brachytherapy is a cost effective form of cancer therapy whereby localized radiation is delivered via devices implanted directly into a tumor or into a tumor cavity following surgery The CivaSheet brachytherapy could minimize exposure of healthy tissue to radiation thus reducing treatment induced side effects while potentially delivering a higher dose of radiation to the target tissues compared to external beam radiation treatment In this grant application we propose to investigate the use of the CivaSheet in pancreatic cancer