Full Press Release Details
Published Article Reporting Clinical Activity of Orally Administered OKT3, a Mouse Anti-CD3 Monoclonal Antibody, in Moderate to
Severe Ulcerative Colitis Patients, Supports Tiziana's Oral Monoclonal Antibody Platform
party research conducted by leading U.S. institutions to be published in a peer reviewed journal Crohn's & Colitis 360
shows orally administered anti-CD3 resulted in anti-inflammatory gene expression with no serious treatment related adverse events
up to a dose of 1 mg of OKT3
platform oral monoclonal antibody (mAb) technology applicable to mAb's on the market today which are currently available
only through IV, addressing an enourmous market potential.
Foralumab is the first fully human anti-CD3 mAb which has not shown anti-drug antibody (immune reaction) in humans
York/London, 24 June 2019 - Tiziana Life Sciences plc (Nasdaq: TLSA / AIM: TILS) ("Tiziana" or the "Company"),
a biotechnology company focusing on the discovery and development of innovative therapeutics for inflammation and oncology indications,
notes the advance publication of a scientific article by third party researchers in the peer reviewed journal Crohn's
& Colitis 360* titled, "Immunologic alterations associated with oral delivery of anti-CD3 (OKT3)
monoclonal antibodies in patients with moderate-to-severe ulcerative colitis"(1) The published study was conducted
at some of the leading medical research institutions in the world, including Harvard Medical School, Massachusetts General Hospital,
and the Ann Romney Center for Neurologic Diseases at Brigham & Women's Hospital. These independent findings suggest
potential clinical activity and support the safety of monoclonal antibodies (mAb's) when administered orally.
Foralumab, the only fully human anti-CD3 mAb, exhibits potency and functionality similar to OKT3, which is a mouse anti-CD3 (2).
Therapeutic use of intravenously administered OKT3 and other humanized anti-CD3 mAbs is limited due to significant adverse reactions,
including life threatening cytokine release syndrome. The Company is pioneering oral delivery of mAb's for the treatment
of autoimmune and inflammatory diseases that is applicable to the $100 billion market of mAb's that are currently only available
through IV delivery.
safe and effective oral delivery of mAb's has the potential to transform the use of biologic medications. While the scientific
community has long recognized oral delivery of proteins and peptides as a challenge, we believe our propeitary platform technology
is a breakthrough in oral delivery of mAb's," stated Kunwar Shailubhai, CEO & CSO of Tiziana. "We are pleased
to see that some of the top researchers in the world are now validating the concept of oral administration of mAbs. Oral administration
with Foralumab may have the potential to deliver superior safety and efficacy results in autoimmune and inflammatory diseases
such as NASH and Crohn's disease."
is currently in a Phase 1 trial at the Harvard Medical School in healthy volunteers to study safety, tolerability and biomarkers
of neurodegenerative disease through nasal delivery. An upcoming Phase 1 trial will evaluate oral Foralumab's safety, tolerability
and biomarkers in Crohn's disease and NASH. A Phase 2 trial in Crohn's and NASH is expected to commence next year.
aim of this pilot study was to determine the immunologic effects and safety of orally delivered anti-CD3 antibody in patients
with moderate-to-severe ulcerative colitis (UC). (1)
primary endpoints were changes in immunologic parameters and evaluation for safety. Six subjects received oral OKT3. The biologic
effects of oral anti-CD3 included significantly increased proliferation in response to anti-CD3 and anti-inflammatory gene expression
profile in peripheral blood mononuclear cells. No serious treatment-related adverse events occurred.
E. K., Canavan, J. B., Moran, C. J., McCann, K., Dunn, W. A., Farraye, F. A., Ananthakrishnan, A. N., Yajnik, V., Gandhi, R.,
Nguyen, D. D., Bhan, A. K., Weiner, H. L., Korzenik, J. R., Snapper, S. B. Immunologic alterations associated with oral delivery
of anti-CD3 (OKT3) monoclonal antibodies in patients with moderate-to-severe ulcerative colitis. Crohn's & Colitis
360 (2019). 183: 240-246.
S1, Preston-Hurlburt P1, Ogura H1, Shailubhai K2, Kuhn C3, Weiner
HL3, Herold KC4. Oral treatment with foralumab, a fully human anti-CD3 monoclonal antibody, prevents
skin xenograft rejection in humanized mice. Clin Immunol. 2017 Oct;183:240-246. doi: 10.1016/j.clim.2017.07.005. Epub 2017
(formerly NI-0401), the only entirely human anti-CD3 mAb, has shown reduced release of cytokines after IV administration in patients
with Crohn's disease, with decreases in the classic side effects of cytokine release syndrome (CRS), and enhances the overall
safety profile of Foralumab. In a humanized mouse model , it was shown that while targeting the T cell receptor, orally administered
Foralumab modulates immune responses of the T cells, enhances Tregs and thus has the potential to provide 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.
(Orthoclone OKT3) is a murine anti-human CD3 monoclonal antibody. OKT3 was developed by Johnson and Johnson and it was the first
monoclonal antibody approved by the FDA in 1985 to be administered to humans via the intravenous route for the trearment of acute,
glucocorticoid-resistant rejection of allogenic renal, heart and liver transplants. However, manufacture of OKT3 was voluntarily
withdrawn from the market.
Tiziana Life Sciences
Life Sciences plc is a UK biotechnology company that focuses on the discovery and development of novel molecules to
treat human disease in oncology and immunology. In addition to Milciclib, the Company is also developing Foralumab for liver diseases.
Foralumab is the only fully human anti-CD3 monoclonal antibody in clinical development in the world. This Phase 2 compound has
potential application in a wide range of autoimmune and inflammatory diseases, such as nonalcoholic steatohepatitis (NASH), primary
biliary cholangitis (PBS), ulcerative colitis, multiple sclerosis, type-1 diabetes (T1D), inflammatory bowel disease (IBD), psoriasis
and rheumatoid arthritis, where modulation of a T-cell response is desirable.