STRUCTURE: KUR-113 Bone Graft Versus Local Autograft for the Treatment of Single-level Transforaminal Lumbar Interbody Fusion

• Sponsor: Kuros Biosurgery AG (Industry)
• Overall Status: Recruiting
• CT.gov ID: NCT04294004
• Collaborator: Factory CRO (Industry), Kuros BioSciences B.V. (Industry)
• Enrollment: 50
• Locations: 16
• Arms: 3
• Anticipated Duration (Months): 49.1
• Patients Per Site: 3.1
• Patients Per Site Per Month: 0.1

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of KUR-113 Bone Graft (TGplPTH1-34 in fibrin) compared to local autograft for the treatment of Degenerative Disk Disease (DDD).

Condition or Disease	Intervention/Treatment	Phase
Degenerative Disc Disease; Spinal Fusion	Combination Product: TGplPTH1-34 in fibrin; Other: Autologous Bone Graft	Phase 2

Detailed Description

Degenerative disc disease (DDD) is a common disorder of the lumbar spine. Clinically, DDD causes discogenic back pain and may cause related radicular, neuropathic, claudicatory, and referred pain.

This is a prospective, randomized, controlled, single-blind, dose-finding, multi-center study which intends to demonstrate the safety and efficacy of KUR-113 Bone Graft (TGplPTH1-34 in fibrin) versus local autograft. The study will enroll 50 patients with Degenerative Disk Disease (DDD) requiring single-level interbody fusion along with posterolateral fusion (PLF) with posterior fixation who meet eligibility criteria and agree to participate in the study. Safety and efficacy of KUR-113 Bone Graft will be evaluated by analyzing all clinical as well as radiological endpoints and adverse events. This phase 2a study is not powered to detect non-inferiority. All patients will undergo clinical and radiological assessments at initial hospital discharge (on average 3 days post-surgery), 6 weeks, 3, 6, 12 and 24 months.

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 50 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Single (Participant)
• Masking Description: Due to the different technical procedures between the control and the intervention arms (KUR-113 Bone Graft versus local autograft), investigators cannot be blinded to the treatment. However, all patients will remain blinded for the duration of their participation in the study.
• Primary Purpose: Treatment
• Official Title: A Prospective, Randomized, Controlled, Single-blind, Dose-finding, Multi-center, Parallel Group Study of Safety/Efficacy of KUR-113 Bone Graft Versus Local Autograft for the Treatment of Single-level Transforaminal Lumbar Interbody Fusion
• Actual Study Start Date: Aug 27, 2020
• Anticipated Primary Completion Date: Sep 30, 2023
• Anticipated Study Completion Date: Sep 30, 2024

Arms and Interventions

Arm	Intervention/Treatment
Experimental: KUR-113, Stage 1 During stage 1, subjects randomized to this arm will receive TGplPTH1-34 in fibrin (0.4mg/ml) that will be applied within and around a polyetheretherketone (PEEK) intervertebral cage. The maximum dose that will be applied is 4 mg of TGplPTH1-34 in 10mL KUR-113 Bone Graft.	Combination Product: TGplPTH1-34 in fibrin; TGplPTH1-34 within a fibrin matrix applied within and around a polyetheretherketone (PEEK) intervertebral cage; Other Names: KUR-113
Active Comparator: Autologous Bone Graft During stage 1 of the study, subjects randomized to this arm will receive local autologous bone graft. In the event of insufficient local autograft, Iliac crest bone graft may be used to supplement.	Other: Autologous Bone Graft; Local autograft collected from decompression which may be supplemented with iliac crest bone graft (ICBG) if local autograft is insufficient.
Experimental: KUR-113, Stage 2 During stage 2, subjects will receive TGplPTH1-34 in fibrin that will be applied within and around a PEEK intervertebral cage at a concentration of either 0.2mg/ml or 0.7mg/ml. The concentration received will be selected by the DSMB based on the results of stage 1. The maximum dose that will be applied is either 2 mg or 7 mg of TGplPTH1-34 in 10mL KUR-113 Bone Graft.	Combination Product: TGplPTH1-34 in fibrin; TGplPTH1-34 within a fibrin matrix applied within and around a polyetheretherketone (PEEK) intervertebral cage; Other Names: KUR-113

Outcome Measures

Primary Outcome Measures

1. Radiographic interbody fusion [Month 12 post-surgery]

   Evidence of bridging trabeculae or continuous bony connection between superior and inferior vertebral body on CT-scan as determined by an independent radiology expert panel (IREP).

Secondary Outcome Measures

1. Composite Endpoint [Month 6 and Month 12 post-surgery]

   Radiographic interbody fusion using CT-scans, functional outcome (decrease of 15 points or more on Oswestry Disability Index (ODI)) and no post-surgical intervention to aid fusion or replace any of the spinal implants.

2. Radiographic interbody fusion [Month 6 post-surgery]

   Determined by IREP using CT-scans

3. Radiographic posterolateral fusion [Month 6 and Month 12 post-surgery]

   Determined by IREP using CT-scans

4. ODI [Week 6, Month 3, Month 6, Month 12, and Month 24 post-surgery]

   Change from baseline

5. Leg Pain [Initial discharge from hospital (on average 3 days post-surgery), Week 6, Month 3, Month 6, Month 12, and Month 24 post-surgery]

   Change from baseline using Visual Analogue Scale (VAS). VAS is scored from 0 to 100 with higher numbers being a worse outcome than a lower number.

6. Back Pain [Initial discharge from hospital (on average 3 days post-surgery), Week 6, Month 3, Month 6, Month 12, and Month 24 post-surgery]

   Change from baseline using Visual Analogue Scale (VAS). VAS is scored from 0 to 100 with higher numbers being a worse outcome than a lower number.

7. Number of Secondary Interventions [Up to Month 24 post-surgery]

   Revisions, re-operations, removals, supplemental fixations, or any other procedure that adjusts or in any way removes part of the original implant configuration with or without replacement of the components

Eligibility Criteria

Criteria

• Ages Eligible for Study: 25 Years to 75 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

1. Written informed consent by the patient.

2. Male or female patient ≥ 25 up to and including 75 years old. Females of childbearing potential with a negative urine pregnancy test at Screening. Females of childbearing potential must agree to use acceptable contraception for at least 12 months after surgery and investigational product placement.

3. Patients with degenerative disc disease with up to grade 1 spondylolisthesis and with leg pain requiring up to 3 levels of laminectomy/decompression and a single-level fusion (L2 - S1). DDD is defined by the presence of one or more of the following:

4. instability (angulation ≥ 5 degrees or translation ≥ 3 mm on flexion/extension radiographs),

5. osteophyte formation of facet joints or vertebral endplates,

6. decreased disc height by > 2 mm, but dependent upon the spinal level,

7. scarring/thickening of ligamentum flavum, annulus fibrosis or facet joint capsule,

8. disc degeneration and/or herniation,

9. facet degeneration,

10. vacuum phenomenon.

11. Patients with an Oswestry Disability Index (ODI) score ≥ 35.

12. Patients with a Visual Analogue Scale (VAS) leg score ≥ 40.

13. Failed conservative treatment (physical therapy, bed rest, medications, spinal injections or transcutaneous electrical nerve stimulation) for a period of 6 months prior to study enrollment.

14. Patients willing to undergo PK sampling.

Exclusion Criteria:

1. Patients with open epiphyseal plates.

2. Patient requiring emergency spinal decompression or spinal fusion.

3. Patients requiring multilevel fusion or expected to need secondary intervention within one year following surgery.

4. Any prior fusion or attempted fusion at an adjacent level.

5. Any prior fusion or attempted fusion at the index level.

6. Pregnant or breast-feeding women.

7. Known or suspected allergies to any of the components of KUR-113 Bone Graft (e.g.

hypersensitivity to aprotinin).

1. Any prior use of teriparatide or abaloparatide or graft material containing PTH1-34.

2. Patients with hypercalcemic disorders (e.g., primary hyperparathyroidism).

3. Patients with Paget's Disease or unexplained high levels of alkaline phosphatase.

4. Prior radiation therapy involving bone.

5. Medical history or radiographic evidence of a metabolic bone disorder (e.g. Paget's Disease) or other condition that would negatively impact the healing process.

6. Any medical condition requiring radiotherapy or immunosuppression.

7. History of thyroid autoimmune disease (Hashimoto's thyroiditis, Graves' disease) or hyperthyroidism.

8. Patients on chronic systemic steroids (i.e. > 14 consecutive days) within 6 months prior to Screening Visit.

9. Osteopenia (T score < -1.0) or osteoporosis of the spine (T score < -2.5).

10. DDD related to benign or malignant tumor.

11. History or presence of active malignancy.

12. Hereditary disorders predisposing to osteosarcoma.

13. Patients with invasive skin cancer.

14. Evidence of local or systemic infection.

15. Patients with known active COVID-19 disease.

16. Current smokers.

17. Type 1 diabetes (regardless of HbA1c) or Type 2 diabetes with a documented HbA1c > 7.0.

18. Any acute or chronic concurrent medical conditions that in the Investigator's opinion are a contraindication to the procedure and study participation.

19. Participation in another investigational study within 30 days prior to surgery for investigational devices, or within the last three months for investigational drugs. (Note: trials requiring extended follow-up for products that were investigational, but have since become commercially available, are not considered investigational trials).

20. Known substance abuse, psychiatric disorder or a condition which, in the opinion of the investigator, may influence the healing or ability to comply with protocol requirements.

21. Involved in active litigation relating to his/her spinal condition or workers compensation claimants.

22. BMI greater than 40.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	University of California San Diego	La Jolla	California	United States	92093-0863
2	Cedars Sinai Medical Center	Los Angeles	California	United States	90048
3	Justin Parker Neurological Institute	Boulder	Colorado	United States	80303
4	MedStar Georgetown University Hospital	Washington	District of Columbia	United States	20007
5	Augusta University Medical Center	Augusta	Georgia	United States	30912
6	Northwestern University-Northwestern Memorial Hospital	Chicago	Illinois	United States	60611
7	Indiana Spine Group	Carmel	Indiana	United States	46032
8	University of Kansas Medical Center (KUMC)	Kansas City	Kansas	United States	66160
9	Spine Institute of Louisiana	Shreveport	Louisiana	United States	71101
10	Brigham and Women's Hospital	Boston	Massachusetts	United States	02115
11	Washington University in St. Louis	Saint Louis	Missouri	United States	63110
12	Hospital for Special Surgery	New York	New York	United States	10021
13	University at Buffalo Neurosurgery	Williamsville	New York	United States	14221
14	Ohio State University Wexner Medical Center	Columbus	Ohio	United States	43201
15	Hospital of the University of Pennsylvania	Philadelphia	Pennsylvania	United States	19104
16	Allegheny General Hospital	Pittsburgh	Pennsylvania	United States	15212

Sponsors and Collaborators

• Kuros Biosurgery AG
• Factory CRO
• Kuros BioSciences B.V.

Investigators

• Principal Investigator: John Chi, MD, Brigham and Women's Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Kuros Biosurgery AG
• ClinicalTrials.gov Identifier: NCT04294004
• Other Study ID Numbers: KUR-113/01
• First Posted: Mar 3, 2020
• Last Update Posted: Aug 11, 2022
• Last Verified: Dec 1, 2021

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Kuros Biosurgery AG: Spinal Fusion; Posterolateral Fusion; MagnetOs; Fibrin-PTH (KUR-113)
• Additional relevant MeSH terms: Intervertebral Disc Degeneration

Study Results

No Results Posted as of Aug 11, 2022