TIDMTILS
Tiziana Life Sciences PLC
30 March 2021
Tiziana Plans Phase 2 Clinical Study in Moderate to Severe
Covid-19 Patients with Nasal Administration of Foralumab, a Fully
Human Anti-CD3 Monoclonal Antibody
-- Since the anti-inflammatory effect of the nasally
administered Foralumab is through the modulation of the immune
system and not by directly targeting Covid-19, this therapeutic
approach could be useful for newly identified Covid-19 variants in
the UK, South Africa and Brazil.
-- Foralumab is the first monoclonal antibody that can be dosed
nasally or orally, due to its ability to effect systemic immunity
via the epithelial lining of the nose, respiratory tract and
gut.
-- The direct rapid delivery of Foralumab to the nasal passage
and respiratory tract was shown in a previous study of mild to
moderate Covid-19 patients to suppress lung inflammation, as
evident from CT scans and reduced systemic markers of inflammation
including interleukin-6 and C-reactive protein.
New York/London, 30 March 2021 - Tiziana Life Sciences plc
(Nasdaq: TLSA / LSE: TILS) ("Tiziana" or the "Company"), a
biotechnology company focused on innovative therapeutics for
oncology, inflammation, and infectious diseases, reports that it
plans further development of Foralumab, its proprietary anti-CD3
human monoclonal antibody in Covid-19. A recent clinical study in
mild to moderate Covid-19 patients showed evidence that the nasally
administered anti-CD3 monoclonal antibody reduced pulmonary and
systemic inflammation and it was well tolerated. That study was
completed in collaboration with scientific teams at the Harvard
Medical School (Boston, USA), and INTRIALS, a full-service Latin
American CRO based in São Paulo, Brazil. Tiziana now plans a phase
2 randomized, placebo-controlled trial in Brazil for moderate to
severe hospitalized Covid-19 patients to test the drug in a more
compromised group of patients. All patients will receive standard
of care background therapy.
Recent studies suggest that the pathogenesis of pulmonary
inflammation in Covid-19 includes an abnormal host response or
overreaction of the immune system in patients. Therefore, nasal
treatment with Foralumab, a fully human anti-CD3 mAb, to modulate
the immune system and to stimulate Tregs is a scientifically
logical approach for the treatment of Covid-19. Foralumab is also
the only monoclonal antibody that can be dosed nasally or orally
due to its ability to effect systemic immunity via the epithelial
lining of the nose, respiratory tract and gut.
"I am pleased to see this novel dosing concept for anti-CD3
advance to a phase 2 clinical trial. These types of human trials
are important to validate the successful studies we conducted in
animal models of several inflammatory diseases," said Professor
Howard Weiner, the Robert L. Kroc Professor of Neurology at the
Harvard Medical School, Director and Founder of the Partners
Multiple Sclerosis Center, and Co-Director of the Ann Romney Center
for Neurologic Diseases at the Brigham & Women's Hospital.
This study is expected to serve as a further proof of concept
for Foralumab's novel method of nasal delivery, as well as its
safety and efficacy as a potent, systemic anti-inflammatory
therapeutic in more severe Covid-19 patients.
Covid-19 enters through the nasal and respiratory passage;
accordingly, the proprietary nasal formulation and nasal delivery
of Foralumab to modulate immunity are expected to delay progression
of the disease and to provide immediate relief to Covid-19
patients.
Dr Neil Graham, Chief Medical Officer at Tiziana Life Sciences,
commented, "We are excited about this next important step in our
goal to validate our drug candidate and our novel delivery system
as a promising and innovative approach to immunomodulatory therapy
for Covid-19 and other mutant variants. By focusing on moderating
the inflammatory consequences of the SARS CoV2 virus, we hope to
have a therapy that has efficacy irrespective of local viral
variants."
About Foralumab
Foralumab (formerly NI-0401), the only entirely human anti-CD3
mAb, shows reduced release of cytokines after IV administration in
patients with Crohn's disease with decreases in the classic side
effects of cytokine release syndrome and improves the overall
safety profile of Foralumab. In a humanized mouse model (NOD/SCID
IL2<GAMMA>c-/-), it was shown that whilst targeting the T
cell receptor, orally administered Foralumab modulates immune
responses of the T cells, enhances regulatory T-cells (Tregs) and
thus provides therapeutic benefit in treating inflammatory and
autoimmune diseases without the occurrence of potential adverse
events usually associated with parenteral mAb therapy (Ogura M. et
al., 2017). Based on animal studies, the nasal and oral
administration of Foralumab offers the potential for the
immunotherapy of autoimmune and inflammatory diseases in a safe
manner by the induction of Tregs.
About Tiziana Life Sciences
Tiziana Life Sciences plc is a dual listed (NASDAQ: TLSA &
LSE: TILS) biotechnology company that focuses on the discovery and
development of novel molecules to treat human diseases in oncology,
inflammation and infectious diseases. In addition to Milciclib, the
Company will be shortly initiating Phase 2 studies with orally
administered Foralumab for Crohn's Disease and nasally administered
Foralumab for progressive multiple sclerosis. Foralumab is the only
fully human anti-CD3 monoclonal antibody ("mAb") in clinical
development in the world. This Phase 2 compound has potential
application in a wide range of autoimmune and inflammatory
diseases, such as Crohn's Disease, multiple sclerosis, type-1
diabetes ("T1D"), inflammatory bowel disease ("IBD"), psoriasis and
rheumatoid arthritis, where modulation of a T-cell response is
desirable. The Company is accelerating development of
anti-Interleukin 6 receptor ("IL6R") mAb, a fully human monoclonal
antibody for treatment of IL6-induced inflammation, especially for
treatment of COVID-19 patients.
For further enquiries:
United Kingdom:
Tiziana Life Sciences
plc
Gabriele Cerrone,
Chairman and founder +44 (0)20 7495 2379
United States:
Investors:
Dave Gentry, CEO
RedChip Companies
Inc.
407-491-4498
dave@redchip.com
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