MedPath

MaaT013 As Salvage Therapy in Ruxolitinib Refractory GI-aGVHD Patients

Phase 3
Active, not recruiting
Conditions
Acute Graft Versus Host Disease in Intestine
Steroid Refractory GVHD
Interventions
Registration Number
NCT04769895
Lead Sponsor
MaaT Pharma
Brief Summary

MaaT013 showed interesting results in steroids and ruxolitinib-resistant aGVHD patients with gut involvement (55% ORR at D28) and 47% and 39% OS at 6 and 12 months respectively (Malard 2020), therefore warrant being tested as salvage therapy in steroid and JAK inhibitors-resistant GI-aGvHD patients. Given the absence of an approved 3rd line strategy or 2nd line strategy in ruxolitinib intolerant patients and the extremely poor prognosis of these patients, who are mostly left with no viable therapeutic option, a single-arm open-label design was proposed.

Detailed Description

Standard first-line therapy for the treatment of acute GVHD involves corticosteroids, usually methyl-prednisolone at a dose of 2 mg/kg per day (Martin PJ R. J., 2012; Van Lint MT, 1998). Despite initial responses (around 60%), fewer than half of patients have durable complete responses, and those patients who do not respond or progress after an initial response have high mortality (Weisdorf D, 1990; Alousi AM, 2009; Bolanos-Meade J, 2014). Moreover, prolonged high-dose corticosteroids (CS) exposure is associated with deleterious complications and long-term morbidity (Mohty M, 2010).

For these reasons, there is great interest in identifying effective therapies for corticosteroid-resistant aGvHD and improve outcomes.

Recently, ruxolitinib (Jakafi®), which has an Orphan Drug status in the USA, was granted an approval on 24 May 2019 from the FDA based on study INCB 18424-271 (NCT02953678). This open-label, single-arm study enrolled 72 grade 2-4 SR-aGvHD patients who were treated with 5 mg (possibly increased to 10mg) ruxolitinib b.d. Of the 72 patients, 49 were included in the efficacy evaluation that led the FDA to grant market authorization. Of these 49 patients, Overall Response Rate (ORR - Complete + Very Good Partial + Partial Responses) after 28 days was 100%, 40.7% and 44.4% for patients with Grade 2, Grade 3, and Grade 4 aGVHD respectively. The overall survival (OS) estimate at 6 months was 51.0% for the entire cohort.

The more recent REACH2 phase 3 randomized trial (NCT02913261) investigating ruxolitinib versus best available therapy in patients with corticosteroid-refractory acute GVHD has further established the role of ruxolitinib in the treatment of corticosteroid-refractory acute GvHD. The ORR at day 28 was higher in the ruxolitinib than in the control group (62% versus 39%; odds ratio, 2.64; 95%CI, 1.65-4.22; P\<0.001). Similarly, the durable overall response at day 56 was higher in the ruxolitinib than in the control group (40% versus 22%; odds ratio, 2.38; 95% CI, 1.43-3.94; P\<0.001) (Zeiser R, 2020) In the REACH1 and REACH2 trials, 45% and 38% of patients, failed to respond to ruxolitinib at day 28, respectively. Moreover, in the REACH2 trial, the overall response at day 56 after initiation of therapy decreased from 62.3% at D28 after initiation of therapy to 39.4% at D56, suggesting a clear unmet medical need for those patients who failed to respond at D28, or worsened afterwards (Zeiser R. 2020). More importantly, results from the REACH1 trial showed only a 22% probability of survival at 2 months in ruxolitinib-non responder patients (Jagasia 2020).

MaaT013 is made of allogeneic, full-ecosystem pooled biotherapeutic intestinal microbiota manufactured by MaaT Pharma in Lyon, France, according to GMP requirements. The intestinal microbiota material in its natural environment is derived from healthy, strictly-vetted and selected donors, following the European consensus recommendations (Cammarota 2016) with the purpose of minimizing the risk associated with fecal material transplants (FMT) for clinical research. Thus, prior to donation, donors undergo a thorough medical evaluation and laboratory screening including SARS-CoV-2 detection, to avoid any known contamination risk. MaaT013 is administered as an enema.

MaaT013 showed interesting results in steroids and ruxolitinib-resistant aGVHD patients with gut involvement (55% ORR at D28) and 47% and 39% OS at 6 and 12 months respectively (Malard 2020), therefore warrant being tested as salvage therapy in steroid and JAK inhibitors-resistant GI-aGvHD patients. Given the absence of an approved 3rd line strategy or 2nd line strategy in ruxolitinib intolerant patients and the extremely poor prognosis of these patients, who are mostly left with no viable therapeutic option, a single-arm open-label design was proposed.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
66
Inclusion Criteria
  • Age ≥ 18 years old
  • Allo-HSCT with any type of donor, stem cell source, GVHD prophylaxis or conditioning regimen.
  • Acute GvHD episode with GI involvement per MAGIC guidelines (= grades II to IV), with or without involvement of other organs
  • Patients resistant to steroids AND either resistant to OR with intolerance to ruxolitinib OR with contra-indication to ruxolitinib:
Exclusion Criteria
  • Patients with known hypersensitivity to vancomycin or to any of the excipients listed in the corresponding SmPC
  • Patients with active CMV colitis
  • Patients who had previously received other lines of systemic aGvHD treatment other than CS and ruxolitinib.
  • Grade II-IV hyper-acute GvHD
  • Overlap chronic GvHD
  • Relapsed/persistent malignancy requiring rapid immune suppression withdrawal.
  • Active uncontrolled infection according to the attending physician
  • Severe organ dysfunction unrelated to underlying GvHD, including:

Cholestatic disorders or unresolved veno-occlusive disease of the liver (defined as persistent bilirubin abnormalities not attributable to GvHD and ongoing organ dysfunction).

Clinically significant or uncontrolled cardiac disease including unstable angina, acute myocardial infarction within 6 months before Day 1 of study drug administration, New York Heart Association Class III or IV congestive heart failure, circulatory collapse requiring vasopressor or inotropic support, or arrhythmia that requires therapy.

Clinically significant respiratory disease that requires mechanical ventilation support or 50% oxygen.

  • Current or past veno-occlusive disease or other uncontrolled complication unless otherwise agreed in writing by the sponsor.
  • Absolute neutrophil count <500/µL for 3 consecutive days. Use of growth factor supplementation is allowed.
  • Absolute platelet count < 10 000/µL. Use of platelet infusion is allowed.
  • Patient with negative IgG EBV serology.
  • Current or past evidence of toxic megacolon, bowel obstruction or gastrointestinal perforation.
  • Any condition that would, in the investigator's judgment, interfere with full participation in the study, including administration of study drug and attending required study visits; pose a significant risk to the subject; or interfere with interpretation of study data.
  • Known allergy or intolerance to trehalose or maltodextrin.
  • Vulnerable patients such as: minors, persons deprived of liberty, persons in Intensive Care Unit unable to provide informed consent prior to the intervention.
  • Females of childbearing potential should have a negative urine or serum pregnancy test within 72 hours prior to receiving the first dose of study medication. Females of childbearing potential should be willing to use 2 methods of birth control or be surgically sterile or abstain from procreative sexual activity for the course of the study. Females of childbearing potential are those who have not been surgically sterilized or have not been free from menses for >1 year. Males should agree to abstain from procreative sexual activity starting with the first dose of study therapy through the end of the study.
  • Other ongoing interventional protocol that might interfere with the current study's primary endpoint.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
MaaT013MaaT013Route of administration: rectal (enema) Study drug dose: 4 enemas in total: Week 1: * D0-D1: vancomycin pre-treatment (250mg per os, 4 times a day for 2 days) * D2: 1 dose * Between D3 to D5: 1 dose Week 2: 1 dose (7 +/- 2 days after the last dose) Week 3: 1 dose (7 +/- 2 days after the last dose) A supplementary dose can be prescribed in case of GvHD relapse or massive antibiotic use during the study.
Primary Outcome Measures
NameTimeMethod
ORR of gastro intestinal-aGvHDDay 28

Overall Response Rate (Complete Response + Very Good Partial Response + Partial Response)

Secondary Outcome Measures
NameTimeMethod
aGvHD ORRDay 28, Day 56 and Month 3

aGvHD overall response rate (CR, VGPR and PR) for all organs

Duration of responseMonth 12

Duration of response after D28

Survival ratesMonth and Month12

Progression-free survival, relapse-free survival, overall survival, steroid-free survival, immunosuppression-free survival

GI aGvHD ORRDay 56 and Month 3

GI aGvHD overall response rate (CR, VGPR and PR)

Safety and tolerabilityMonth 12

incidence of SAE and key events

chronic GvHD incidence and severityMonth 12

Percentage of chronic GvHD incidence and severity

Best response ratesuntil Month 3

CR, VGPR and PR for GI and overall aGvHD

Trial Locations

Locations (50)

Cliniques Universitaires Saint-Luc

🇧🇪

Brussels, Belgium

CHRU Lille - Hopital Claude Huriez

🇫🇷

Lille, France

Institut Paoli Calmettes

🇫🇷

Marseille, France

Universitatsklinikum Wurzburg

🇩🇪

Würzburg, Germany

Istituto di Ricovero e Cura a Carattere Scientifico - Ospedale Policlinico San Martino

🇮🇹

Genova, Italy

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

🇮🇹

Milano, Italy

Fondazione Policlinico Universitario Agostino Gemelli

🇮🇹

Roma, Italy

Azienda Ospedaliero-Universitaria Citta della Salute e della Scienza di Torino

🇮🇹

Torino, Italy

Medizinische Universität Innsbruck

🇦🇹

Innsbruck, Austria

Ordensklinikum Linz Elisabethinen

🇦🇹

Linz, Austria

Algemeen Ziekenhuis Sint-Jan Brugge-Oostende - Campus Sint-Jan

🇧🇪

Brugge, Belgium

Universitair Ziekenhuis Brussel

🇧🇪

Brussel, Belgium

Universitair Ziekenhuis Gent

🇧🇪

Gent, Belgium

Centre Hospitalier Universitaire de Liège

🇧🇪

Liège, Belgium

Centre Hospitalier Universitaire Amiens-Picardie - Site Sud

🇫🇷

Amiens, France

Centre Hosptitalier Universitaire d'Angers

🇫🇷

Angers, France

CHU de Caen

🇫🇷

Caen, France

Centre Hospitalier Universitaire Grenoble Alpes

🇫🇷

Grenoble, France

Hôpital Lapeyronie

🇫🇷

Montpellier, France

Hôpital l'Archet

🇫🇷

Nice, France

APHP St Antoine

🇫🇷

Paris, France

Hôpital Haut-Lévêque

🇫🇷

Pessac, France

Centre Hospitalier Lyon-Sud

🇫🇷

Pierre-Bénite, France

Centre Hospitalier Universitaire de Poitiers

🇫🇷

Poitiers, France

Hôpital Pontchaillou

🇫🇷

Rennes, France

Institut de Cancérologie Lucien Neuwirth

🇫🇷

Saint-Priest-en-Jarez, France

Institut Universitaire du Cancer de Toulouse Oncopole

🇫🇷

Toulouse, France

Hôpitaux de Brabois

🇫🇷

Vandœuvre-lès-Nancy, France

Helios Klinikum Berlin-Buch

🇩🇪

Berlin, Germany

Universitätsmedizin Mannheim

🇩🇪

Mannheim, Germany

Universitätsklinikum Regensburg

🇩🇪

Regensburg, Germany

Universitätsklinik Ulm - Oberen Eselsberg

🇩🇪

Ulm, Germany

Azienda Ospedaliera Regionale San Carlo

🇮🇹

Ancona, Italy

Azienda Ospedaliero-Universitaria di Bologna Policlinico Sant Orsola-Malpighi

🇮🇹

Bologna, Italy

IRCCS Ospedale San Raffaele

🇮🇹

Milano, Italy

Grande Ospedale Metropolitano Bianchi Melacrino Morelli

🇮🇹

Reggio Calabria, Italy

Presidio Ospedaliero Universitario Santa Maria della Misericordia

🇮🇹

Udine, Italy

Hospital de la Santa Creu i Sant Pau

🇪🇸

Barcelona, Spain

Institut Català d'Oncologia - Hospital Duran i Reynals (ICO L'Hospitalet)

🇪🇸

Barcelona, Spain

Hospital Clínico Universitario Virgen de la Arrixaca

🇪🇸

El Palmar, Spain

Hospital Universitario Virgen de las Nieves

🇪🇸

Granada, Spain

Hospital General Universitario Morales Meseguer

🇪🇸

Murcia, Spain

Hospital Universitario La Paz

🇪🇸

Madrid, Spain

Hospital Universitario Ramón y Cajal

🇪🇸

Madrid, Spain

Clinica Universidad de Navarra - Pamplona

🇪🇸

Pamplona, Spain

Complejo Asistencial Universitario de Salamanca - Hospital Clínico

🇪🇸

Salamanca, Spain

Hospital Universitario Marqués de Valdecilla

🇪🇸

Santander, Spain

Instituto de Biomedicina de Sevilla

🇪🇸

Sevilla, Spain

Hospital Clínico Universitario de Valencia

🇪🇸

Valencia, Spain

Hospital Universitari i Politècnic La Fe

🇪🇸

Valencia, Spain

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