Delving into the Latest Updates on Spinal Restoration, Inc. with Synapse

Overview

The purpose of this investigation is to establish the safety and efficacy of the Biostat System when used for treatment of chronic low back (lumbar) pain due to symptomatic internal disc disruptions (IDD) by comparing safety and efficacy outcome measures between one group receiving BIOSTAT BIOLOGX® Fibrin Sealant through the Biostat® Delivery Device and another group receiving a preservative-free normal saline control delivered with the Biostat Delivery Device.

Start Date01 Mar 2010

Sponsor / Collaborator

Spinal Restoration, Inc.

NCT00693784

/ CompletedNot Applicable

A Multicenter Pilot Study of Resorbable Biologic Disc Augmentation for Treatment of Symptomatic Lumbar Internal Disc Disruption (IDD) With the Biostat® Disc Augmentation System

The purpose of this study is to assess the safety of the Biostat Disc Augmentation System for the treatment of chronic low-back (lumbar) pain due to symptomatic internal disc disruptions (IDD) and to obtain preliminary efficacy information.

Start Date01 Jun 2008

Sponsor / Collaborator

Spinal Restoration, Inc.

100 Clinical Results associated with Spinal Restoration, Inc.

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0 Patents (Medical) associated with Spinal Restoration, Inc.

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100 Deals associated with Spinal Restoration, Inc.

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100 Translational Medicine associated with Spinal Restoration, Inc.

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Pipeline

Pipeline Snapshot as of 15 Jan 2025

The statistics for drugs in the Pipeline is the current organization and its subsidiaries are counted as organizations,Early Phase 1 is incorporated into Phase 1, Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3

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