MaaT Pharma to Present Clinical Data for MaaT013 and MaaT033 at 49th EBMT Annual Meeting
11 April 2023 - 06:00PM
Business Wire
- Data, which were previously presented at the American Society
of Hematology (ASH) Annual Meeting in December 2022, includes
results of 81 patients with gastrointestinal acute
Graft-versus-Host Disease (GI-aGvHD) treated with MaaT013 as part
of a compassionate use program in France, and results of the Phase
1b CIMON trial with the Company’s Microbiome Ecosystem TherapyTM
(MET) oral capsule MaaT033 in acute myeloid leukemia (AML)
patients.
- The Company was selected for two oral presentations at the
conference; presentations will highlight MaaT013 and MaaT033’s
potential to improve survival outcome for patients with
hematological malignancies.
Regulatory News:
MaaT Pharma (EURONEXT: MAAT – the “Company”), a French
clinical-stage biotech and a pioneer in the development of
Microbiome Ecosystem TherapiesTM (MET) dedicated to improving
survival outcomes for patients with cancer, announced that
promising clinical data for its drug candidates, MaaT013 and
MaaT033 will be reported in two oral presentations by Pr.
Florent Malard, Professor of Hematology at the Saint-Antoine
Hospital and Sorbonne University during the 49th Annual Meeting
of the European Society for Blood and Marrow Transplantation (EBMT
2023) to be held as an hybrid event in Paris, France, from April 23
- 26, 2023. The EBMT Annual Meeting is a leading event in Europe
that focuses on cutting-edge scientific content related to
transplantation and cellular therapy. The oral presentations will
include data that were previously presented at the American Society
of Hematology conference in December 2022.
Key clinical findings with MaaT013 as compassionate use in
France (Early Access Program or “EAP”) in 81 patients
- Clinical results showed a GI-Overall Response Rate (ORR) of 56%
including 30 complete responses (37%), 11 very good partial
responses (14%) and 4 partial responses (5%) in GI-aGvHD patients
28 days after treatment initiation; 12-month overall survival was
59% in patients responding to MaaT013 treatment.
- A 65% ORR was observed in 31 patients treated with MaaT013 as
3rd-line therapy after failure to 2nd-line ruxolitinib treatment;
12-month overall survival in this group responding to MaaT013
treatment was 74%; similar patient population is being treated in
MaaT Pharma’s ongoing pivotal Phase 3 ARES clinical trial in
Europe.
Oral Presentation details for MaaT013:
Title: Pooled Fecal Allogenic Microbiotherapy for Refractory
Gastrointestinal Acute Graft-versus Host Disease: Results from the
Early Access Program in France Abstract number: OS05-08 Session
Name: Oral Session 5 | GVHD (Clinical) Date/Time: Wednesday, April
26, 2023 11:33 am - 11:42 am CET Location: Amphithéâtre Bleu
Key clinical findings with MaaT033 in Phase 1b study
CIMON
- MaaT033 was shown to be safe and tolerable in 21 patients; 4
severe adverse events were reported in 4 patients, only one was
considered as possibly related to the treatment by the
investigator.
- Treatment with MaaT033 induced increased microbiota richness
as well as strong and persistent engraftment in cohorts 3 and 4 of
the dose escalation study, which consisted of taking 3 capsules of
the drug candidate per day.
- Engraftment following MaaT033 treatment correlated with
increased anti-inflammatory marker levels and reduced inflammatory
marker levels in patients.
- MaaT Pharma is preparing a randomized, double-blind,
placebo-controlled pivotal Phase 2b clinical trial for MaaT033;
trial start is expected in Q2 2023 as previously announced.
Oral Presentation details for MaaT033:
Title: Restoration of Gut Microbiota Diversity with Oral Pooled
Fecal Microbiotherapy in Acute Myeloid Leukemia Patients after
Intensive Chemotherapy: the Phase 1b CIMON trial Abstract number:
OS06-08 Session Name: Oral Session 6 | Acute Leukemia (II)
Date/Time: Wednesday, April 26, 2023 10:39 am - 10:48 am CET
Location: Maillot
Participants are also invited to meet with MaaT Pharma’s
clinical team at booth #48. All EBMT sessions that take place
onsite will be live-streamed through the congress platform and will
be available on-demand after they are aired live.
Link to register: https://eu.eventscloud.com/ebmt23
About MaaT Pharma
MaaT Pharma, a clinical stage biotechnology company, has
established a complete approach to restoring patient-microbiome
symbiosis in oncology. Committed to treating cancer and
graft-versus-host disease (GvHD), a serious complication of
allogeneic stem cell transplantation, MaaT Pharma has launched, in
March 2022 in Europe, a Phase 3 clinical trial for patients with
acute GvHD, following the achievement of its proof of concept in a
Phase 2 trial. Its powerful discovery and analysis platform,
gutPrint®, supports the development and expansion of its pipeline
by determining novel disease targets, evaluating drug candidates,
and identifying biomarkers for microbiome-related conditions. The
company’s Microbiome Ecosystem Therapies are produced through a
standardized cGMP manufacturing and quality control process to
safely deliver the full diversity of the microbiome, in liquid and
oral formulations. MaaT Pharma benefits from the commitment of
world-leading scientists and established relationships with
regulators to support the integration of the use of microbiome
therapies in clinical practice.
MaaT Pharma is the first company developing microbiome-based
therapies listed on Euronext Paris (ticker: MAAT).
Forward-looking statements
This press release contains forward-looking statements. All
statements other than statements of historical fact included in
this press release regarding future events are subject to (i)
change without notice and (ii) factors beyond the Company's
control. These statements may include, but are not limited to,
statements preceded by, followed by or including words such as
"target", "believe", "expect", "aim", "intend", "may", "forecast",
"estimate", "plan", "project", "will", "may have", "likely",
"should", "expect" 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 differ
materially from those expressed or implied by such forward-looking
statements.
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version on businesswire.com: https://www.businesswire.com/news/home/20230411005747/en/
MaaT Pharma – Investor Relations Hervé AFFAGARD
Co-founder and CEO Siân CROUZET COO / CFO +33 4 28 29 14 00
invest@maat-pharma.com MaaT Pharma – Media Relations Pauline
RICHAUD Senior PR & Corporate Communications Manager +33 6 14
06 45 92 prichaud@maat-pharma.com Trophic Communications
Corporate and Medical Communications Stephanie MAY or Charlotte
SPITZ +49 171 351 2733 maat@trophic.eu
Maat Pharma (EU:MAAT)
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