Tiziana Announces Initiation of Phase 1b Clinical Trial in Crohn's Disease Patients to Evaluate Oral Capsules of Foralumab, a Fully Human Anti-CD3 Monoclonal Antibody This clinical trial, the first-ever oral immunotherap

Tiziana Announces Initiation of Phase 1b

Clinical Trial in Crohn's Disease Patients to Evaluate Oral Capsules of Foralumab, a Fully Human Anti-CD3 Monoclonal Antibody

New York, March 25, 2022 - Tiziana Life Sciences (Nasdaq:

TLSA) ("Tiziana" or the "Company"), a biotechnology company enabling breakthrough immunotherapies via novel routes

of monoclonal antibody delivery, today announced initiation of a Phase 1b clinical trial to evaluate orally administered enteric-coated

capsules of foralumab in patients with mild-to-moderate Crohn's Disease (CD). This revised protocol,

as previously outlined in the Company's announcement on February 4, 2022, allows

for the study of a broader patient population and a shorter dosing period. These protocol amendments or revisions are intended to expedite

patient enrollment with study completion targeted for the fourth quarter of 2022.

This study is the first multiple-dose study with orally administered

enteric-coated capsules of foralumab in patients with CD. This study will initiate soon with patient enrollment in the second quarter

of 2022. Enteric-coated capsules, containing doses up to 5 mg of foralumab, will be administered once-daily for five consecutive

days to patients with mild-to-moderately active CD. While the primary objective is safety and tolerability, additional endpoints are

to assess clinical and immune signal responses, including calprotectin measurements in stool. Blood samples will be collected to evaluate

pharmacokinetics, including the rate and extent of systemic absorption. The presence of anti-drug antibodies (ADAs) will also be determined.

Typically, therapeutic antibodies

are administered either intravenously or subcutaneously, but severe and sometimes life-threatening side effects may occur. Oral

administration with foralumab is a novel approach to induce an anti-inflammatory immune response via site-targeted immunomodulation in

the gut. Previous mouse and patient studies have demonstrated that orally delivered anti-CD3 antibody effectively ameliorates gut inflammation

in a murine model of colitis1 and in patients with moderate-to-severe ulcerative colitis2. Currently, commonly

used immunotherapies for CD require intravenous or subcutaneous administration of anti-TNF-alpha antibodies, such as HUMIRA

(NASDAQ: ABBV), REMICADE (NASDAQ: JNJ), and anti-CD23 antibodies (STELARA )(NASDAQ: JNJ).

Dr. Kunwar Shailubhai, Chief Executive Officer and Chief Scientific Officer

of Tiziana, commented, "The oral route of administration is the preferred route for all pharmaceuticals. The "Holy Grail"

for biologics is the "switch" from parenteral (IV, SC) to oral administration as it is the most economical, non-invasive,

and convenient route with respect to patient's quality of life and compliance. We have developed proprietary formulation technologies,

enabling oral, nasal, and inhalation routes for administration of antibodies, to facilitate local action at the respective target sites.

We believe this Phase 1b study is a logical first step towards the clinical validation of oral immunotherapy with foralumab capsules,

to provide local action rather than systemic delivery, for CD treatment."

Howard Weiner, M.D., Director of the Multiple Sclerosis Program at the

Brigham and Women's Hospital (BWH) and Chairman of Tiziana's Scientific Advisory Board, commented, "Treatment with orally

or nasally administered foralumab is a novel physiological approach to stimulate the mucosal immune system to induce disease-modifying

benefits while minimizing the toxicities that are commonly associated with the traditional intravenous or subcutaneous immunotherapies.

In this regard, the first validation of our innovative approach came from our recently reported clinical results showing positive clinical

benefits in a patient with secondary progressive multiple sclerosis (SPMS), who was treated for 6 months with intranasally administered

Foralumab (TZLS-401; formerly NI-0401), the only entirely human anti-CD3

mAb, shows reduced release of cytokines after IV administration in healthy volunteers and in patients with Crohn's disease. In a humanized

mouse model (NOD/SCID IL2 c-/-), it was shown that while targeting the T-cell receptor, orally administered foralumab modulates

immune responses of the T-cells and enhances regulatory T-cells (Tregs), thereby providing therapeutic benefit in treating inflammatory

and autoimmune diseases without the occurrence of potential adverse events usually associated with parenteral mAb therapy (Ogura et al.,

Clin. Immunol. 183:240-246, 2017). Once a day treatment for 10 consecutive days with

intranasal foralumab was not only well tolerated but also produced strong clinical responses in COVID-19 patients (Moreira et al., Front

Immunol 12: 709861,2021). Based on these studies, the intranasal and oral administration of foralumab offers the potential to

become a well-tolerated immunotherapy for autoimmune and inflammatory diseases by the induction of Tregs.

About Crohn's Disease

Crohn's Disease (CD) is a chronic inflammatory bowel disease that affects the digestive tract lining. CD affects men, women, and

children and up to a half-million people in the U.S. The CD typically appears in younger people - often in their late teens, 20s,

or early 30s. However, this condition can happen at any age. CD cannot be cured, but medications such as steroids and immunosuppressants

are used to slow its progression. If these medications aren't effective, a patient may require surgery. CD is also considered an autoimmune

disease caused by dysregulation of the immune system.

About Tiziana Life Sciences

Tiziana Life Sciences is a clinical-stage biopharmaceutical company developing

breakthrough therapies using transformational drug delivery technologies to enable alternative routes of immunotherapy. Tiziana's innovative

nasal, oral, and inhalation approaches in development have the potential to provide an improvement in efficacy as well as safety and

tolerability compared to intravenous (IV) delivery. Tiziana's two lead candidates, intranasal foralumab, the only fully human anti-CD3

mAb, and milciclib, a pan-CDK inhibitor, have both demonstrated a favorable safety profile and clinical response in patients in studies

to date. Tiziana's technology for alternative routes of immunotherapy has been patented with several applications pending and is expected

to allow for broad pipeline applications.

Forward-Looking Statements

Certain statements made in this announcement are forward-looking statements. These forward-looking statements are not historical facts

but rather are based on the Company's current expectations, estimates, and projections about its industry; its beliefs; and assumptions.

Words such as 'anticipates,' 'expects,' 'intends,' 'plans,' 'believes,' 'seeks,' 'estimates,' and similar expressions are intended to

identify forward-looking statements. These statements are not guarantees of future performance and are subject to known and unknown risks,

uncertainties, and other factors, some of which are beyond the Company's control, are difficult to predict, and could cause actual results

to differ materially from those expressed or forecasted in the forward-looking statements. The Company cautions security holders and

prospective security holders not to place undue reliance on these forward-looking statements, which reflect the view of the Company only

as of the date of this announcement. The forward-looking statements made in this announcement relate only to events as of the date on

which the statements are made. The Company will not undertake any obligation to release publicly any revisions or updates to these forward-looking

statements to reflect events, circumstances, or unanticipated events occurring after the date of this announcement except as required

by law or by any appropriate regulatory authority.

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