RECONFIRM - Study of AGN1 LOEP in Patients With Osteoporosis

Osteoporosis Clinical Trial

Official title:

Prospective, Post-market Evaluation of Safety and Efficacy of a Local Osteo- Enhancement Procedure (LOEP) in the Proximal Femur of Women in Europe With Osteoporosis

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05202678
• Other study ID #: AGN-CIP-301
• Status: Recruiting
• Phase: N/A
• Start date: July 5, 2021
• Est. completion date: December 2026

Study information

• Verified date: January 2024
• Source: AgNovos Healthcare, LLC
• Contact: Adam Lowe
• Phone: +1 240 753 6500
• Email: info[@]agnovos.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The research will be conducted as a prospective, post-market, multi-center study within Europe. The maximum number of subjects to be treated is 150 across up to 20 sites. This will be a non-randomized and open-label study. The study will collect procedural, short- and long-term data on the safety and clinical performance of AGN1 LOEP in the post-market setting in European countries where AGN1 LOEP is commercially available. AGN1 is intended to form new bone in voids in the proximal femur of women with osteoporosis.

Description:

To qualify for this study, a subject must have at least one intact hip with bone loss attributable to osteoporosis as indicated by a femoral neck DXA T-score of -2.5 or less. Follow-up visits will be conducted at 10 days, 42 days, 12 months, and 24 months after the procedure. Study evaluations at each follow-up visit include general health (physical exam and medical history update), VAS pain (not at 10 days), FES-I (not at 10 days), EQ5D-5L and Parker Mobility. A Timed Up and Go Test is performed at the 10-day, 42-day and 12-month follow-up. Patient satisfaction with outcome of surgery will be asked at the 42-day and the 12-month follow-up. DXA scans and X-rays will be performed at 12 and 24 months.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 150
• Est. completion date: December 2026
• Est. primary completion date: December 2025
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

1. Subject is a postmenopausal female (at least 1-year post menses).

2. Subject has bone loss in the hip attributable to osteoporosis as defined by a femoral neck DXA T-score of -2.5 or less.

3. Subject has at least one hip without previous surgery or fracture.

4. Subject is medically stable from any previous treatment or medical procedure in the opinion of the investigator and with an ASA score of I or II.

5. Subject has willingness, ability, and commitment to participate in baseline and follow-up evaluations for the full length of the study.

6. Subject is capable of giving written informed consent to participate in the study.

Exclusion Criteria:

1. Subject is less than 3 months removed from having a hip fracture repair or prosthesis or elective Total Hip Arthroplasty (THA).

2. Subject has progressive increase in hip pain over the previous six (6) months that in the opinion of the Investigator suggests moderate to severe intra-articular arthritis, labral tear, extraarticular soft tissue pathology, referred pain, tumor, stress fracture or infection.

3. Subject is dependent on the use of a wheelchair or is bedridden.

4. Subject has albumin corrected serum calcium levels outside the normal lab range or has a pre-existing calcium metabolism disorder (e.g., hypercalcemia).

5. Subject has severe renal insufficiency defined as an estimated glomerular filtration rate (eGFR) < 30 mL/min or is being treated with dialysis.

6. Subject has hemoglobin A1c level = 7.5%.

7. Subject has Body Mass Index (BMI) > 35.

8. Subject exhibits excessive smokeless tobacco use or excessive smoking as determined by the principal investigator*.

9. Subject is at ASA Class III, IV, V or VI.

10. Subject exhibits excessive alcohol consumption as determined by the principal investigator*.

11. Subject has radiological evidence of gross bony or joint pathology of the hip, including signs predictive of atypical femoral fractures (e.g., Cortical beaking) or has been diagnosed and/or treated for atypical femoral fractures.

12. Subject treated with corticosteroids or systemic glucocorticoids for ten (10) days in the previous six (6) months.

13. Subject has history of oral or parenteral use of immunesuppressive drugs in the previous twelve months.

14. Subject has history of metabolic bone disease other than osteoporosis (ex. Paget's disease).

15. Subject has a history of auto-immune arthritic diseases including rheumatoid, psoriatic, or those associated with systemic lupus erythematosus, spondyloarthropathy, Reiter's Syndrome or Crohn's Disease.

16. Subject has a history of radiation therapy to the hip or pelvic region.

17. Subject has a history of any invasive malignancy (except basal cell carcinoma), unless treated and with no clinical signs or symptoms of the malignancy for five (5) years.

18. Subject has known allergies to implanted device.

19. In the judgement of the Investigator, the subject is not a good study candidate (e.g., inability to maintain follow-up schedule, comorbidity or poor general physical/mental health, or drug or alcohol abuse issues).

20. Subject is currently enrolled in another clinical study. *AgNovos's recommendation is >1 pack per day smoking and >3 alcoholic drinks per day

Related Conditions & MeSH terms

• Osteoporosis

Intervention

Device:
• AGN1 LOEP
Subjects with osteoporosis are treated with AGN1 local osteo-enhancement procedure in the proximal femur

Locations

Country	Name	City	State
Belgium	AZ Nikolaas	Sint-Niklaas	Antwerpen

Sponsors (1)

Lead Sponsor	Collaborator
AgNovos Healthcare, LLC

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Bone Formation	Radiologic appearance of bone formation as assessed by X-ray at 12 and 24 months post-procedure of treated hips.	12 and 24 months
Other	Patient Satisfaction	Patient satisfaction with outcome of surgery in the treated hip(s) and overall at 42 days and 12 months assessed with Visual Analogue Scale.	42 days and 12 months
Other	Pain hip	Pain (left hip, right hip) at baseline, 42 days, 12 months, and 24 months assessed with Visual Analogue Scale.	baseline, 42 days, 12 months, and 24 months.
Other	Pain body overall	Pain body overall at baseline, 42 days, 12 months, and 24 months assessed with Visual Analogue Scale.	baseline, 42 days, 12 months, and 24 months.
Other	FES-I	FES-I at baseline, 42 days, 12 months, and 24 months	baseline, 42 days, 12 months, and 24 months
Other	Quality of Life with EQ5D-5L	EQ5D-5L at baseline, 10 days, 42 days, 12 months, and 24 months	baseline, 10 days, 42 days, 12 months, and 24 months
Other	Parker Mobility Score	Parker Mobility Score at baseline, 10 days, 42 days, 12 months, and 24 months.	baseline, 10 days, 42 days, 12 months, and 24 months.
Other	Verifying the enhancement site	The ability to access the enhancement site by drilling through the lateral femoral cortex of the proximal femur and to determine the boundaries of the enhancement site using the probe debrider.	Procedure (day 0)
Other	Technical Success	The ability to deliver the necessary amount of AGN1 material to adequately fill the osseous defect as assessed by the treating surgeon.	Procedure (day 0)
Other	SAE	Incidence of all serious adverse events post-AGN1 LOEP through the 24 months follow-up period.	24 months
Other	Hip Fracture	Incidence of new hip fractures on the treated side.	24 months
Other	Timed up and go test	Timed up and go test at baseline, 10 days, 42 days and 12 months.	baseline, 10 days, 42 days and 12 months.
Primary	Femoral Neck Bone Mineral Density	6% increase in mean femoral neck BMD from preprocedure baseline to 12 months post-procedure of treated hips	12 months
Primary	Primary Safety Evaluation	The incidence of all adverse events and serious adverse events occurring post-AGN1 LOEP through the 12 months follow-up period determined to be at least possibly related to the procedure and/or device.	12 months
Secondary	Total Hip Bone Mineral Density	6% increase in mean total hip BMD from preprocedure baseline to 12 months post-procedure of treated hips.	12 months
Secondary	Femoral Neck Bone Mineral Density	6% increase in mean femoral neck BMD from preprocedure baseline to 24 months post-procedure of treated hips.	24 months
Secondary	Total Hip Bone Mineral Density	6% increase in mean total hip BMD from preprocedure baseline to 24 months post-procedure of treated hips.	24 months