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Citius Submits Mino-Wrap Briefing Package to FDA for Pre-IND Consult

- Mino-Wrap being developed for the reduction of post-operative infections associated with breast reconstruction surgery - Mino-Wrap is the second major drug

articleCitius Pharmaceuticals, Inc.August 4, 20204/company/citius-pharmaceuticals-inc/news/citius-submits-mino-wrap-briefing-package-to-fda-for-pre-ind-consult
Citius Submits Mino-Wrap Briefing Package to FDA for Pre-IND Consult

About this update from Citius Pharmaceuticals, Inc.

[{"type":"text","content":"- Mino-Wrap being developed for the reduction of post-operative infections associated with breast reconstruction surgery\n - Mino-Wrap is the second major drug development collaboration with MD Anderson Cancer Center\n\n\nCRANFORD, N.J., Aug. 4, 2020 /PRNewswire/ -- Citius Pharmaceuticals, Inc. (\"Citius\") (\"Company\") (NASDAQ: CTXR), a specialty pharmaceutical company focused on adjunctive cancer care and critical care drug products announced progress in the development of Mino-Wrap, a novel approach to reducing post-operative infections associated with surgical implants.\nMino-Wrap is a gel-containing minocycline and rifampin film that is used to wrap the tissue expander (\"TE\") used in breast reconstructive surgeries. In order to stimulate early consultation and potentially speed the development of Mino-Wrap, the company has submitted a briefing package to the FDA Division of Anti-Infective Products. The briefing package contains information regarding pre-clinical data and a clinical development plan, along with questions for the FDA regarding safety and efficacy data that would be required to advance Mino-Wrap into clinical trials. The company will consider the feedback provided by the FDA in the development of the Pre-IND. There is no set timeline for FDA to respond to a consultation package; however, based on pre-COVID-19 experience, we expect a response from FDA within 60 days.\nMino-Wrap also marks the second collaboration with MD Anderson Cancer Center (\"MDACC\") who are the inventors of this novel approach to preventing post-mastectomy infections when tissue expanders are used. The Company is currently developing Mino-LokĀ®, an antibiotic lock treatment for catheter-related bloodstream infections (CRBSIs), in collaboration with MDACC. Mino-Lok is in phase 3 development. \n\"The published rate of infection for tissue expanders used in breast reconstructive surgery is between 2.5 % and 24%, with an estimated mean at around 12% to 14%. We believe Mino-Wrap has the potential to provide a significant reduction in the incidence of infection, sparing the patient the pain and discomfort of extended hospitalization and further aggressive and lengthy courses of antibiotics in an attempt to salvage the TEs. In many cases the TE is removed leading to a delay in lifesaving chemo-radiation therapy, which can be a devastating cons...

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