Subcutaneous Injections of Autologous ASC to Heal Digital Ulcers in Patients With Scleroderma. (ADUSE)

• ClinicalTrials.gov Identifier: NCT04356755
• Recruitment Status: Recruiting
• First Posted: April 22, 2020
• Last Update Posted: October 27, 2020
• Sponsor: University Hospital, Toulouse
• Information provided by (Responsible Party): University Hospital, Toulouse

Study Description

Brief Summary:

Ischemic digital ulcers (DUs) are a frequent complication in systemic sclerosis with a major impact on hand function and quality of life. Digital injection of autologous cultured adipose-derived stromal constitutes a promising approach to treat scleroderma-induced refractory ischemic DUs where no alternative therapy is validated. The aim of this phase 2 study is to compare efficacy and safety of digital injection of autologous cultured adipose-derived stromal cell versus placebo for healing refractory active ischemic digital ulcers in patients with systemic sclerosis.

Condition or disease	Intervention/treatment	Phase
Systemic Sclerosis	Procedure: Adipose tissue harvest; Drug: Autologous ASC; Drug: Placebo	Phase 2

Detailed Description:

Systemic sclerosis (SSc) is a systemic autoimmune disease characterized by an autoimmune-mediated microangiopathy and progressive fibrosis. Ischemic digital ulcers (DUs) are frequent in the disease course. DUs are an expression of the severity of the microangiopathy. DUs lead to pain, infection, gangrene, autoamputation, impaired hand use and impaired quality of life. The management of DUs is often based on optimal wound care to promote healing and and repeated hospitalizations to perform onerous prostacyclin infusions to reduce pain and accelerate healing. With optimal standard of care, only 60% of DUs are healed after 3 months and 46.2% experiences recurrence during that time among them 11.2% experiences a chronic evolution. No drug has demonstrated a positive effect on refractory DUs healing. The rational underlying the use of cultured adipose-derived stromal cell (ASC) in this indication is based on the finding of ASC, in vitro and in vivo, angiogenic and anti-inflammatory potential in other ischemic pathologies, with an excellent safety profile. The pilot phase of the ACellDREAM trial demonstrated the feasibility and safety of autologous ASC transplantation in patients with non- revascularizable critical limb ischemia and showed improvement in ulcer evolution and wound healing. The EFS-O culture procedure safety is validated and is already in use in ongoing French and European clinical trials. Two pilot studies showed the safety of autologous adipose tissue grafting for scleroderma-Induced DU. The SCLERADEC pilot study outlines the safety, in 12 SSc patients, of the digital injection of adipose- derived autologous stromal vascular fraction, which is a heterogeneous population of cells including only 36% of uncultured ASC. An improvement in hand disability, quality of life and DUs was observed, the phase II is ongoing. The hypothesis of the study is that digital injection of autologous cultured adipose-derived stromal cell could be efficacious for scleroderma-induced refractory ischemic DUs healing by digital vascular regeneration in a clinical situation where no alternative therapy is validated.

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 32 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
• Primary Purpose: Treatment
• Official Title: Subcutaneous Injections of Autologous Cultured Adipose-derived Stroma/ Stem Cells to Heal Refractory Ischemic Digital Ulcers in Patients With Scleroderma
• Actual Study Start Date: September 22, 2020
• Estimated Primary Completion Date: March 2023
• Estimated Study Completion Date: March 2023

Arms and Interventions

Arm	Intervention/treatment
Experimental: autologous cultured ASC; Subcutaneous injections of autologous cultured adipose-derived stroma/stem cells to heal refractory ischemic digital ulcers in patients with scleroderma	Procedure: Adipose tissue harvest; An adipose tissue harvest (1) will be performed at D-14±1 for patient from arm ASC. Patients from placebo arm will have a sham adipose tissue harvest.; Drug: Autologous ASC; At day 0, patients will have ASC injections(3) in their ischemic DU. Patients will be followed-up for 16 weeks
Placebo Comparator: Placebo; Subcutaneous injections of placebo comparator to heal refractory ischemic digital ulcers in patients with scleroderma	Drug: Placebo; At day 0, patients will have placebo injections(3) in their ischemic DU. Patients will be followed-up for 16 weeks

Outcome Measures

Primary Outcome Measures :

1. Proportion of refractory active ischemic digital ulcers healed (complete or partial) [ Time Frame: 16 weeks ]
   Partial healing is defined as > 50% reduction of the DU area or > 50% re epidermisation of the DU.
2. Composite endpoint combining healing (complete or partial) without recurrence and without local or general complications [ Time Frame: 16 weeks ]

   Partial healing is defined as > 50% reduction of the DU area or > 50% re epidermisation of the DU.

   Local complications resulting from DU worsening:

   • Critical ischemic crisis necessitating hospitalization,
   • Gangrene, (auto) amputation,
   • Failure of conservative management: Surgical and chemical sympathectomy, vascular reconstructions, or any unplanned surgery in the management of hand SSc manifestation(s),
   • Use of parenteral prostanoids after treatment injection,
   • Requiring class II, III or IV narcotics or increase in existing dose of > 50 % as compared to baseline,
   • Initiation of systemic antibiotics for the treatment of infection attributed to digital ulceration.

   General complications will be assessed by:

   • Clinical examination
   • Patient reported-outcomes
   • Laboratory assessments

Secondary Outcome Measures :

1. Percentage of participants with Digital Ulcer complete healing [ Time Frame: 16 weeks ]
   Number of complete ulcer Healing. Complete healing is defined as 100% re-epidermisation.
2. Percentage of participants with Digital Ulcer partial healing [ Time Frame: 16 weeks ]
   Number of partial ulcer Healing. Partial healing is defined as > 50% reduction of the DU area or > 50% re epidermisation of the DU.
3. Percentage of participants with wound surface reduction <50% [ Time Frame: 16 weeks ]
   the wound surface reduction is defined by analysis photography
4. Percentage of participants with new Digital Ulcer [ Time Frame: 16 weeks ]
   Number of patients who do not develop any new DU.
5. Percentage of participants with Digital Ulcer complication [ Time Frame: 16 weeks ]
   A complication is an infection, gangrene, amputation or a DU requiring IV prostanoids.
6. Change from Baseline in Pain Scores [ Time Frame: 16 weeks ]
   Evaluation of pain on a Visual Analog Scale. The visual scale measures the intensity of pain on a scale ranging from 0 (no pain) to 10 (maximum pain).
7. Change from Baseline in severity of Raynaud's phenomenon [ Time Frame: 16 weeks ]
   Change in severity of Raynaud's phenomenon on a Visual Analog Scale. The visual scale is in a form of plastic ruler and measures the severity of Raynaud's phenomenon on a scale ranging from 0 (no pain) to 100 (maximum pain).
8. Change from Baseline in Digital ischaemia [ Time Frame: 16 weeks ]
   Change in digital ischaemia of the treated fingers on Digital arterial pressure.
9. Change from Baseline in cutaneous ischaemia [ Time Frame: 16 weeks ]
   Change in cutaneous ischaemia of the treated fingers on transcutaneous oxygen pressure (TcPO2).
10. Change from Baseline in Digital microvascular organisation [ Time Frame: 16 weeks ]
    Change in digital microvascular organisation of the treated fingers on nailfold capillaroscopy.
11. Change from Baseline in hand functional disability [ Time Frame: 16 weeks ]
    Evaluation of hand functional disability by the Cochin Hand Function Scale.
12. Change from Baseline in quality of life in systemic sclerosis [ Time Frame: 16 weeks ]
    Evaluation of quality of life in systemic sclerosis by scleroderma health assesment (SHAQ).
13. Change from Baseline in quality of life [ Time Frame: 16 weeks ]
    Evaluation of quality of life by the SF36.
14. Change from Baseline in health status [ Time Frame: 16 weeks ]
    Evaluation of health status by the EQ5D.
15. Vascular biomarkers [ Time Frame: 16 weeks ]
    Endothelin-1, Endostatin, Endogline, Angiotensin I and II, Tie 1 and 2, V-EGF, sICAM-1, sVCAM, E-selectin, CXCL4 plus anti-AT1R, anti-ETAR, anti Annexin V will be measured out in blood samples by Luminex

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Male or female patient ≥18 years of age,
• Patient with systemic sclerosis according to the 2013 ACR/EULAR classification criteria9,
• SSc patient with at least one refractory active ischemic digital ulcer at "inclusion visit" (see below the eligibility conditions of a DU),
• Age > 50 years and not treated with any kind of hormone replacement therapy for at least 2 years prior to screening, with amenorrhea for at least 24 consecutive months prior to screening. An assessment of serum follicle stimulating hormone showing a level of > 40 TU/L at screening may be used to exclude childbearing potential, based on the discretion of the investigator,
• Patient must have provided written informed consent prior to enrolment,
• Patient must be able to understand their requirements of participating in the protocol,
• Patient affiliated to a social security system.
• Relative to each DU :

The DU at " inclusion visit " must show all the following characteristics:

1. Located beyond the proximal interphalangeal joint, on finger surface (included periungual ulcers),
2. Of ischemic origin according to the physician,
3. Not over subcutaneous calcifications or bone relief,
4. Active DU,
5. Refractory after 10±2 weeks of standard of care according to EULAR recommendations26 (that is either still active (chronic) or new occurrence despite standard of care)

Exclusion Criteria:

• Current smoker or tobacco consumption stopped for less than 3 months prior to inclusion, - Patient participating in a clinical trial or having participated in a clinical trial within the previous 3 months,
• Patients on statins, who have received treatment for less than 3 months prior to Screening or whose treatment has not been stable during this period,
• Patients on vasodilators, such as endothelin receptor antagonists (ERAs), PDE5 inhibitors (e.g. sildenafil, tadalafil), calcium channel blockers, ACE-inhibitors, nitroglycerin, alpha adrenergic blockers, or angiotensin II receptor antagonists, N-acetylcysteine, antiplatelet aggregation therapy and low molecular weight heparin who have received treatment if present for less than 3 months prior to "inclusion visit" or whose treatment has not been stable for at least 1 month prior to "inclusion visit",
• Treatment with disease modifying agents such as methotrexate, mycophenolate mofetil, azathioprine, tacrolimus, Interferons and cyclophosphamide, those drugs should be stop at least 1 month prior study entry.
• Treatment with oral corticosteroids (> 10 mg/day of prednisone or equivalent),
• Systemic antibiotics (oral and TV) to treat infected DU(s) within 4 weeks prior to "inclusion visit",
• Use of topical growth factors, hyperbaric oxygen,
• Local injection of botulinum toxin in an affected finger within 4 weeks prior to "inclusion visit",
• Surgical sympathectomy of the upper limbs or surgical wound debridement within 1 month prior to "inclusion visit",
• Liposuction technically impossible,
• Patient who underwent autologous hematopoietic stem cell transplantation (HSCT) within less than 1 year,
• Patients with an indication for intensification by autologous HSCT (according to EBMT guidelines and national RCP MATHEC),
• History of cancer in the last five years, except for successfully excised basal cell/squamous cell carcinoma, or successfully excised early melanoma of the skin. Subjects, who had successfully tumor resection or radiation or chemotherapy more than 5 years from inclusion and no recurrence, may be enrolled in the study, - Subjects who have active proliferative retinopathy,
• Positive HIV-1 or 2, HTLV-1 or 2, HBV or HCV,
• Patients with a history of stroke, myocardial infarction or severe arrhythmia in the last 6 months
• Patient who had severe cardiac failure in the last 6 months,
• Females who are pregnant or breastfeeding or plan to do so during the course of this study,
• Patient under judicial protection, - Refusal of the patient to participate in the study.

• Relative to each DU:

  1. Digital ulcer due to conditions other than scleroderma,
  2. Non ischemic digital ulcer,
  3. Ulcers with osteomyelitis, or clinically uncontrolled infection,
  4. Infected digital ulcer requiring systemic antibiotherapy,
  5. Digital ulcer requiring urgent surgery.

Contacts and Locations

Contacts

Contact: Grégory PUGNET, MD, PHD; 05 61 77 71 26 ext +33; pugnet.g@chu-toulouse.fr

Locations

France

Grenoble Hospital; Not yet recruiting

Grenoble, France

Contact: Bernard IMBERT

Lille Hopsital; Not yet recruiting

Lille, France

Contact: Eric Hachulla

Marseille Hospital; Not yet recruiting

Marseille, France

Contact: Brigitte Granel

Montpellier Hospital; Not yet recruiting

Montpellier, France

Contact: Philippe GILPAIN

Nantes Hospital; Not yet recruiting

Nantes, France

Contact: Christian AGARD

Poitiers Hospital; Not yet recruiting

Poitiers, France

Contact: Mathieu Puyade

CHU de Toulouse - Hôpital PURPAN-TSA; Recruiting

Toulouse, France, 31059

Contact: Grégory PUGNET, MD, PHD 05 61 77 71 26 ext +33 pugnet.g@chu-toulouse.fr

Sponsors and Collaborators

University Hospital, Toulouse

Investigators

• Principal Investigator: Grégory PUGNET, MD, PHD

More Information

• Responsible Party: University Hospital, Toulouse
• ClinicalTrials.gov Identifier: NCT04356755
• Other Study ID Numbers: RC31/17/0447
• First Posted: April 22, 2020
• Last Update Posted: October 27, 2020
• Last Verified: October 2020

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:

Scleroderma, Systemic; Scleroderma, Diffuse; Connective Tissue Diseases; Skin Diseases