Full Press Release Details
Pharmaceuticals Reaches 92 Event Milestone in Mino-Lok Phase 3 Trial
N.J., August 10, 2023 -- Citius Pharmaceuticals, Inc. ("Citius" or the "Company") (Nasdaq: CTXR), a late-stage
biopharmaceutical company dedicated to the development and commercialization of first-in-class critical care products, today announced
that it has reached an important milestone in its clinical trial for Mino-Lok , an antibiotic lock solution to salvage
catheters in patients with catheter-related bloodstream infections. Pending confirmation from an adjudication committee of independent
reviewers, the Company believes all 92 events required to complete the trial have been achieved. Several patients remain in active treatment,
which may result in additional events.
is a significant milestone for Citius as we approach completion of the Phase 3 Mino-Lok trial. As we complete therapy for patients in
active treatment, we will continue to enroll patients in the pipeline and initiate shutdown activities," stated Leonard Mazur,
Chairman and Chief Executive Officer of Citius.
Phase 3 Trial Design
Mino-Lok Phase 3 pivotal superiority trial (NCT02901717) is a multi-center, randomized, open-label, blinded study to determine the efficacy
and safety of Mino-Lok (MLT), a novel antibiotic lock therapy that combines minocycline with edetate disodium. The trial is being conducted
in the U.S. and India. The primary endpoint for this study is the time (in days following randomization) to a catheter failure event
between randomization and TOC (Week 6) in the Intent-to-Treat (ITT) Population. Additional secondary outcome measures include overall
success, microbiological eradication, and clinical cure, among others.
diagnosed with catheter related blood stream infections (CRBSI/CLABSI) and who meet all necessary criteria for the study are randomized
in a 1:1 ratio to receive either Mino-Lok therapy or standard of care antibiotic lock therapy.
in the Mino-Lok arm receive one MLT dose daily with a dwell time of two to four hours for a total of seven doses. For subjects in the
Control arm, the investigator determines the antibiotic used in the lock, dose, dwell time, and number of days of administration based
on institutional standards or Infectious Diseases Society of America (IDSA) guidelines.
is an antibiotic lock solution to treat patients with catheter-related blood stream infections that Citius has licensed from The University
of Texas MD Anderson Cancer Center. Citius believes Mino-Lok provides a superior alternative to removing and replacing a central venous
catheter (CVC), leading to a reduction in serious adverse events and cost savings to the healthcare system. If approved, Mino-Lok would
be the first and only FDA-approved treatment that salvages central venous catheters that cause central line-related blood stream infections.
Citius Pharmaceuticals, Inc.
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's
diversified pipeline includes two late-stage product candidates, Mino-Lok, an antibiotic lock solution for the treatment of patients
with catheter-related bloodstream infections, which is currently enrolling patients in a Phase 3 Pivotal superiority trial, and LYMPHIR
(E7777), a novel IL-2R immunotherapy for an initial indication in CTCL. Mino-Lok was granted Fast Track designation by the FDA.
LYMPHIR received orphan drug designation by the FDA for the treatment of CTCL and PTCL. At the end of March 2023, Citius completed enrollment
in its Phase 2b trial of CITI-002, a topical formulation for the relief of hemorrhoids. For more information, please visit www.citiuspharma.com.
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 "will," "anticipate,"
"estimate," "expect," "plan," "should," and "may" and other words and terms of similar
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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: risks relating to the results of research and development activities,
including those from existing and new pipeline assets, including Mino-Lok; our need for substantial additional funds; the estimated markets
for our product candidates and the acceptance thereof by any market; the ability of our product candidates to impact the quality of life
of our target patient populations; our ability to commercialize our products if approved by the FDA; our ability to obtain, perform under
and maintain financing and strategic agreements and relationships; uncertainties relating to preclinical and clinical testing; the early
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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 identify, acquire, close and integrate product candidates and companies successfully and on a timely
basis; 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 and could be impacted by any future public health risks. 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
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