CORRECTING and REPLACING: MaaT Pharma Presented Positive Updated Data on MaaT013 in the Early Access Program at ASH 2024 Annual Meeting
10 Dezember 2024 - 2:30AM
Business Wire
MaaT Pharma to host a KOL webinar on December
17th, 2024, to discuss data and the unmet medical need in acute
Graft-versus-Host Disease (aGvHD) - Register here.
- Sustained High Response Rates at Day 28: Gastrointestinal
Overall Response Rate (GI-ORR) was 51% and Overall Response Rate
(ORR) for all organs was 49%.
- Long-Term Survival: Overall Survival (OS) was 47% at 12 months,
and 42% at 24 months.
- [Corrected] Median OS among patients responding to MaaT013
within the ARES-like population was 444 days, compared to 42 days
in non-responders. Historically, median OS to best available
therapy following Ruxolitinib is 28 days (Abedin et al.,
2021).
- Topline results for the ARES pivotal Phase 3 trial anticipated
in January 2025.
Regulatory News:
This replaces the announcement made at 18:00 CET on 9 December
2024 due to the following corrections: Updated subheadline.
MaaT Pharma Presented Positive Updated Data
on MaaT013 in the Early Access Program at ASH 2024 Annual
Meeting
MaaT Pharma to host a KOL webinar on December
17th, 2024, to discuss data and the unmet medical need in acute
Graft-versus-Host Disease (aGvHD) - Register here.
- Sustained High Response Rates at Day 28: Gastrointestinal
Overall Response Rate (GI-ORR) was 51% and Overall Response Rate
(ORR) for all organs was 49%.
- Long-Term Survival: Overall Survival (OS) was 47% at 12 months,
and 42% at 24 months.
- Median OS among patients responding to MaaT013 within the
ARES-like population was 444 days, compared to 42 days in
non-responders. Historically, median OS to best available therapy
following Ruxolitinib is 28 days (Abedin et al., 2021).
- Topline results for the ARES pivotal Phase 3 trial anticipated
in January 2025.
MaaT Pharma (EURONEXT: MAAT – the “Company”), a clinical-stage
biotechnology company and a leader in the development of Microbiome
Ecosystem Therapies™ (MET) dedicated to enhancing survival for
patients with cancer through immune modulation, announced that
Prof. Malard, MD, hematology professor at Saint-Antoine Hospital
and Sorbonne University, today detailed updated data for 154
patients with acute Graft-versus-Host Disease (aGvHD) treated with
MaaT013 in Early Access Program (EAP) in Europe during the 66th
American Society of Hematology (ASH) Annual Meeting.
Speaking on the data, Florent Malard, MD, PhD, highlighted:
“These findings underscore MaaT013’s potential as a transformative
therapy for aGvHD, a condition with poor survival rates and limited
treatment options. The high response rates and long-term survival
data further validate the critical role of the gut microbiome
modulation in managing aGvHD. Additionally, these results highlight
the growing interest within the medical community, as demonstrated
by ASH's dedicated symposium on the microbiome’s role in
transplantation and cellular therapies."
Hervé Affagard, CEO and co-founder of MaaT Pharma, added: “The
high demand from clinicians demonstrates growing adoption and trust
in MaaT013. The strong real-world data from our Early Access
Program not only gives us confidence as we approach Phase 3 results
but also validates our immune modulation approach through
microbiome-based therapies. Success in GvHD, a severe and complex
immune-mediated disease, would pave the way to demonstrate the
platform's potential to address a broad range of complex
immune-related diseases."
As a reminder, key findings include:
For the full cohort (154 patients) in the EAP
- Durable response: 51% GI-ORR at Day 28 and a 44% GI-ORR at Day
56. ORR for all organs was 49% at D28 and 42% at D56.
- Overall survival (OS): 53% at 6 months, 47% at 12 months, and
42% at 24 months.
- Median survival follow-up: 418 days (range, 27–1644 days).
Subset (n=58) resembling the population enrolled in the Phase 3
ARES trial (receiving 2nd line ruxolitinib):
- Higher response rate than the full cohort: GI-ORR was 59% at
Day 28 and 54% at D56. ORR considering all organ was 55% at D28,
and 56% at D56.
- OS was 54% at 6 months, 49% at 12 months, and 40% at 24 months
vs 15% at 12 months in published historical data (Abedin et al. Br
J Haematol. 2021 Nov).
Full details on data available here.
Upcoming events & milestones:
- MaaT Pharma will host a webcast on December 17th, 2024, at
6.00pm CET/ 12.00pm ET/ 9.00am PT to discuss the latest EAP data,
detailing the high unmet medical need and the upcoming milestones
for MaaT013. To attend, please register here.
- Topline results for the pivotal Phase 3 ARES trial
(NCT04769895), completed in October 2024, are expected in January
2025 and should further validate MaaT013’s potential in meeting
high unmet medical need for patients with aGvHD with no therapeutic
options.
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 Therapy™ for acute,
hospital use. It is characterized by a consistently high diversity
and richness of microbial species and the presence of Butycore™
(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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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
Catalytic Agency – Media Relations Heather Shea Media
relations for MaaT Pharma +1 617-286-2013
heather.shea@catalyticagency.com
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