Full Press Release Details
Citius Pharmaceuticals,
Inc. Holds Pre-BLA Meeting with the FDA for I/ONTAK (denileukin diftitox) for the Treatment of Cutaneous T-Cell Lymphoma
Biologics License Application (BLA) submission
planned for the second half of 2022
CRANFORD, N.J., July 12, 2022 -- Citius
Pharmaceuticals, Inc. ("Citius" or the "Company") (Nasdaq: CTXR), a late-stage biopharmaceutical company developing
and commercializing first-in-class critical care products, today announced that the Company held a Type B pre-BLA meeting with the
U.S. Food and Drug Administration (FDA) to discuss I/ONTAK (denileukin diftitox), an engineered IL-2-diphtheria toxin fusion protein for
the treatment of patients with persistent or recurrent cutaneous T-cell lymphoma (CTCL). I/ONTAK is a purified and more bioactive formulation
of previously FDA-approved ONTAK . The pre-BLA meeting was held with representatives from the FDA's Center for Drug
Evaluation and Research (CDER).
The purpose of the pre-BLA meeting with the
FDA was to discuss the content and acceptability of the Company's anticipated BLA for I/ONTAK. The briefing document provided to
the FDA included a review of clinical and non-clinical studies and previous meeting minutes with the FDA.
"We appreciate the FDA's continued
guidance on the development path of a more purified formulation of ONTAK. Based on the FDA's pre-BLA meeting comments, we intend
to move forward with our planned BLA submission for I/ONTAK in the second half of 2022. We look forward to continued engagement with the
FDA as we advance this program to provide CTCL patients with a potential new treatment option," stated Leonard Mazur, Chairman and
I/ONTAK is a recombinant fusion protein that
combines the interleukin-2 (IL-2) receptor binding domain with diphtheria toxin fragments. The agent specifically binds to IL-2 receptors
on the cell surface, causing diphtheria toxin fragments that have entered cells to inhibit protein synthesis. I/ONTAK, a purified version
of denileukin diftitox, is a reformulation of previously FDA-approved oncology treatment ONTAK. ONTAK was marketed in the U.S. from 1999
to 2014, when it was voluntarily withdrawn from the market. Manufacturing improvements resulted in a new formulation, which maintains
the same amino acid sequence but features improved purity and bioactivity. The new formulation received regulatory approval in Japan for
the treatment of CTCL and PTCL. In 2011 and 2013, the FDA granted orphan drug designation (ODD) to I/ONTAK for the treatment of PTCL and
CTCL, respectively, making it potentially eligible for seven years of market exclusivity post-approval for each indication.
About Cutaneous T-cell Lymphoma
Cutaneous T-cell lymphoma is a type of cutaneous
non-Hodgkin lymphoma (NHL) that comes in a variety of forms and is the most common type of cutaneous lymphoma. In CTCL, T-cells, a type
of lymphocyte that plays a role in the immune system, become cancerous and develop into skin lesions, leading to a decrease in the quality
of life of patients with this disease due to severe pain and pruritus. Mycosis Fungoides (MF) and S zary Syndrome (SS) comprise
the majority of CTCL cases. Depending on the type of CTCL, the disease may progress slowly and can take anywhere from several years to
upwards of ten to potentially reach tumor stage. However, once the disease reaches this stage, the cancer is highly malignant and can
spread to the lymph nodes and internal organs, resulting in a poor prognosis. Given the duration of the disease, patients typically cycle
through multiple systemic agents to control disease progression. CTCL affects men twice as often as women and is typically first diagnosed
in patients between the ages of 50 and 60 years of age. Other than allogeneic stem cell transplantation, for which only a small fraction
of patients qualify, there is currently no curative therapy for advanced CTCL. Approximately 3,000 new cases are reported in the United
States every year, with an estimated 30,000 - 40,000 individuals living with the disease.
About Citius Pharmaceuticals, Inc.
Citius is a late-stage biopharmaceutical company
dedicated to the development and commercialization of first-in-class critical care products, with a focus on oncology, anti-infectives
in adjunct cancer care, unique prescription products, and stem cell therapies. The Company has two late-stage product candidates, Mino-Lok ,
an antibiotic lock solution for the treatment of patients with catheter-related bloodstream infections (CRBSIs), which is currently enrolling
patients in a Phase 3 Pivotal superiority trial, and I/ONTAK (E7777), a novel IL-2R immunotherapy for an initial indication in cutaneous
T-cell lymphoma (CTCL), for which a BLA submission is being prepared for the second half of 2022. Mino-Lok was
granted Fast Track designation by the U.S. Food and Drug Administration (FDA). I/ONTAK has received orphan drug designation by the FDA
for the treatment of CTCL and peripheral T-cell lymphoma (PTCL). For more information, please visit www.citiuspharma.com.
This press release may contain "forward-looking
statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934.
Such statements are made based on our expectations and beliefs concerning future events impacting Citius. You can identify these statements
by the fact that they use words such as "believe," "anticipate," "estimate," "expect," "plan,"
"should," and "may" and other words and terms of similar meaning or use of future dates. Forward-looking statements
are based on management's current expectations and are subject to risks and uncertainties that could negatively affect our business,
operating results, financial condition and stock price. Factors that could cause actual results to differ materially from those currently
anticipated are: we may experience delays or unexpected hurdles in our efforts to submit a BLA for I/ONTAK and we may not be able to
submit the BLA on the timelines we expect or at all; the FDA may find inadequacies and deficiencies in our BLA for I/ONTAK, including
in the data we submit, and may decide not to accept the BLA for filing; our ability to successfully undertake and complete clinical and
non-clinical trials and the results from those trials for our product candidates; the estimated markets for our product candidates and
the acceptance thereof by any market; our ability to commercialize our products if approved by the FDA; our dependence on third-party
suppliers; the ability of our product candidates to impact the quality of life of our target patient populations; risks relating to the
results of research and development activities, including those from existing and new pipeline assets; uncertainties relating to preclinical
and clinical testing; our need for substantial additional funds; the early stage of products under development; market and other conditions;
our ability to attract, integrate, and retain key personnel; risks related to our growth strategy; patent and intellectual property matters;
our ability to obtain, perform under and maintain financing and strategic agreements and relationships; our ability to identify, acquire,
close and integrate product candidates and companies successfully and on a timely basis; our ability to procure cGMP commercial-scale
supply; government regulation; competition; as well as other risks described in our SEC filings. These risks have been and may be further
impacted by Covid-19. Accordingly, these forward-looking statements do not constitute guarantees of future performance, and you are cautioned
not to place undue reliance on these forward-looking statements. Risks regarding our business are described in detail in our Securities
and Exchange Commission ("SEC") filings which are available on the SEC's website at www.sec.gov, including in our Annual
Report on Form 10-K for the year ended September 30, 2021, filed with the SEC on December 15, 2021 and updated by our subsequent filings
with the SEC. These forward-looking statements speak only as of the date hereof, and we expressly disclaim any obligation or undertaking
to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in our expectations
or any changes in events, conditions or circumstances on which any such statement is based, except as required by law.
Investor Relations for Citius Pharmaceuticals:
Vice President, Investor Relations and Corporate Communications
T: 908-967-6677 x113