18F-FP-DTBZ for PET Imaging of Beta Cell Mass in Diabetes

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$247,050.00
Award Year:
2007
Program:
SBIR
Phase:
Phase I
Contract:
1R43DK079416-01
Award Id:
85586
Agency Tracking Number:
DK079416
Solicitation Year:
n/a
Solicitation Topic Code:
n/a
Solicitation Number:
n/a
Small Business Information
AVID RADIOPHARMACEUTICALS, INC., 3624 Market Street, 5th Floor, Philadelphia, PA, 19104
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
170631720
Principal Investigator:
DANIELSKOVRONSKY
(484) 716-0886
SKOVRONSKY@AVIDRP.COM
Business Contact:
() -
skovronsky@avidrp.com
Research Institute:
n/a
Abstract
DESCRIPTION (provided by applicant): Both Type I (T1D) and Type 2 (T2D) diabetes share a common pathophysiology - insufficient beta cell mass (BCM) to meet metabolic demands. Unfortunately, advances in diabetes are slowed by a lack of reliable methods to m easure BCM in vivo. The ability to accurately track BCM would facilitate development and clinical evaluation of therapies to preserve or replace beta cells. To date, one of the most exciting emerging technologies for measuring BCM is positron emission tomo graphy (PET) imaging using C-DTBZ, a tracer which binds to the vesicular monoamine transporter (VMAT-2) 11 expressed in beta cells in pancreatic islets. While ground-breaking studies have recently demonstrated proof of concept for C-DTBZ imaging of BCM, th e applicability for human studies is limited since the 11 short half-life of C (20 min.) means that C-DTBZ clinical studies are only feasible at a limited number of centers with on-site cyclotrons. Since the PET isotope F has a 110 min. half life and has a well 18 established nationwide distribution network, an F version of DTBZ would represent an incredibly 18 powerful and widely accessible tool for the study of diabetes. We have now developed an F derivative of DTBZ (18F-FP-DTBZ or F-AV-133) and have alre ady completed (or have in progress) all the necessary IND-enabling studies on F-FP-DTBZ. In this SBIR grant we propose to conduct the first ever clinical trial of F-FP-DTBZ in T1D and T2D patients and rapidly test the hypothesis that F-FP-DTBZ is a useful biomarker for PET imaging of BCM. 18 Successful development of a biomarker for beta cell mass (BCM) would represent a significant milestone and a large commercial opportunity for diagnostic imaging of diabetic and pre-diabetic patients. Vesicular monoamin e transporter (VMAT-2) is expressed in beta cells in pancreatic islets and is the target for dihydrotetrabenazine (DTBZ). We have now synthesized a highly potent and efficacious derivative of DTBZ, AV-133 for VMAT-2 binding. 18 F-AV-133 is a first of its k ind F- 18 labeled VMAT-2 targeting radiotracer that will be utilized to in a proof of concept clinical trial to image BCM in normal control and Type 1 and Type 2 diabetics. This imaging-based biomarker may represent a significant advance in diabetes manage ment by allowing better diagnosis, disease monitoring, and therapeutic selection. Avid Radiopharmaceuticals is an experienced leader in developing new commercial PET tracers, is collaborating with world-experts on VMAT-2 imaging, and is first company with a promising F lead compound, F-AV-133, for imaging VMAT-2 expressed on beta cells.

* information listed above is at the time of submission.

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