MaaT Pharma Completes Recruitment of its ARES Phase 3 Trial for MaaT013 to Treat Acute Graft-versus-Host Disease
15 10월 2024 - 2:30PM
Business Wire
- Last patient treated in MaaT Pharma’s Phase 3 ARES clinical
trial
- Topline results publication now expected in January 2025
- Positive DSMB review of Phase 3 ARES trial announced in Q4
2023, with a favourable benefit/risk ratio and "high efficacy and
low toxicity"
- Registration process to commence with submission expected in
2025 in Europe
Regulatory News:
MaaT Pharma (EURONEXT: MAAT – the “Company”), a clinical-stage
biotechnology company and a leader in the development of Microbiome
Ecosystem TherapiesTM (MET) dedicated to enhancing survival for
patients with cancer through immune modulation, today announced
full recruitment of its Phase 3 clinical trial designed to evaluate
efficacy and safety of its lead asset MaaT013 in the treatment of
steroid refractory and ruxolitinib refractory or intolerant acute
Graft-versus-Host Disease (aGvHD) (NCT04769895). This achievement
is one of the most significant milestones in the Company’s
development and the study’s topline results, including the primary
endpoint (Gastrointestinal aGvHD Overall Response Rate) are now
expected to be released in January 2025.
Hervé Affagard, CEO and co-founder of MaaT Pharma stated:
“Completing the enrolment of this Phase 3 marks a major milestone
in our mission to improve outcomes for blood cancer patients and
underscores our continued commitment to the GvHD community. MaaT013
enables immune modulation by optimizing the gut microbiota balance
while lowering the risk of adverse events associated with
conventional immunosuppressive therapies. We are confident that
MaaT013 could become the first-ever approved therapy harnessing
microbiome-driven immune modulation in oncology, opening the door
to the creation of a new therapeutic pillar across a broad range of
cancer types.”
ARES is a pivotal Phase 3 multicenter, European, open-label,
single-arm study assessing the safety and efficacy of MaaT013 in
patients with GI-aGvHD refractory to steroids and ruxolitinib. The
study anticipated recruiting a maximum of 75 patients to account
for potential dropouts and the Company has reached its goal by
enrolling 66 evaluable patients, the number required for an
accurate assessment of the primary endpoint. The Company previously
announced in Q4 2023 the positive outcome of the interim Data
Safety Monitoring Board (DSMB) of the Phase 3 ARES trial, including
a favourable benefit/risk ratio, with “high efficacy and low
toxicity.” In parallel, MaaT013 has been available for the past 5
years in Early Access Program in 6 countries in Europe to treat
acute Graft-versus-Host Disease, with over 180 patients safely
treated as of today.
Next steps and milestones for MaaT013 in GvHD:
- Early December 2024: Company to host Key Opinion Leaders
discussion on updated data from Early Access Program in Europe for
MaaT013 in treating aGvHD.
- January 2025:
- Topline results with primary endpoint evaluation: GI Overall
Response Rate (GI-ORR) at day 28
- Company to host Key Opinion Leaders discussion on Phase 3
data
- By end of 2025: Secondary endpoint evaluation including
One-year Overall Survival
About MaaT Pharma
MaaT Pharma is a leading, late-stage clinical company focused on
developing innovative gut microbiome-driven therapies to modulate
the immune system and enhance cancer patient survival. Supported by
a talented team committed to making a difference for patients
worldwide, the Company was founded in 2014 and is based in Lyon,
France.
As a pioneer, MaaT Pharma is leading the way in bringing the
first microbiome-driven immunomodulator in oncology. Using its
proprietary pooling and co-cultivation technologies, MaaT Pharma
develops high diversity, standardized drug candidates, aiming at
extending life of cancer patients. MaaT Pharma has been listed on
Euronext Paris (ticker: MAAT) since 2021.
About MaaT013
MaaT013 is a full-ecosystem, off-the-shelf, standardized,
pooled-donor, enema Microbiome Ecosystem TherapyTM for acute,
hospital use. It is characterized by a consistently high diversity
and richness of microbial species and the presence of ButycoreTM
(group of bacterial species known to produce anti-inflammatory
metabolites). MaaT013 aims to restore the symbiotic relationship
between the patient’s functional gut microbiome and their immune
system to correct the responsiveness and tolerance of immune
functions and thus reduce steroid-resistant, gastrointestinal
(GI)-predominant aGvHD. MaaT013 has been granted Orphan Drug
Designation by the US Food and Drug Administration (FDA) and the
European Medicines Agency (EMA).
About acute Graft-versus-Host Disease
Acute Graft-versus-Host Disease occurs in patients within 100
days of undergoing a stem cell or bone marrow transplant. The
transplanted cells attack the recipient, causing inflammation of
the skin, liver and/or gastro-intestinal tract. GI-aGvHD results in
patients experiencing very high volumes of diarrhea which can be
life-threatening. The standard first line therapy for treating
aGvHD is the use of systemic steroids. If patients do not respond
to steroids, they are considered Steroid Resistant (SR) and other
agents can be administered. Currently the only agent approved for
treating SR aGvHD after failure of steroid treatment is
ruxolitinib, which is currently approved for this indication in USA
and has received approval from the European Medical Agency’s
Committee for Human Medicinal Products (CHMP) on March 25,
2022.
Forward-looking Statements
All statements other than statements of historical fact included
in this press release about future events are subject to (i) change
without notice and (ii) factors beyond the Company’s control. These
statements may include, without limitation, any statements preceded
by, followed by, or including words such as “target,” “believe,”
“expect,” “aim”, “intend,” “may,” “anticipate,” “estimate,” “plan,”
“project,” “will,” “can have,” “likely,” “should,” “would,” “could”
and other words and terms of similar meaning or the negative
thereof. Forward-looking statements are subject to inherent risks
and uncertainties beyond the Company’s control that could cause the
Company’s actual results or performance to be materially different
from the expected results or performance expressed or implied by
such forward-looking statements.
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version on businesswire.com: https://www.businesswire.com/news/home/20241014925613/en/
MaaT Pharma – Investor Relations Guilhaume DEBROAS, Ph.D.
Head of Investor Relations +33 6 16 48 92 50 invest@maat-pharma.com
MaaT Pharma – Media Relations Pauline RICHAUD Senior PR
& Corporate Communications Manager +33 6 14 06 45 92
media@maat-pharma.com
Maat Pharma (EU:MAAT)
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부터 11월(11) 2024 으로 12월(12) 2024
Maat Pharma (EU:MAAT)
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부터 12월(12) 2023 으로 12월(12) 2024