Melinta Medical Affairs

Clinical Trials

Melinta Therapeutics is committed to researching and developing products that improve patient care and advance medicine.

 See below for a brief description of our ongoing trials. For ongoing clinical trials, visit ClinicalTrials.gov.
 

Phase 3 Multicenter Adult Double-Blind

Melinta has licensed US commercial rights to rezafungin from Mundipharma, which is the sponsor of this study.



Phase 1 Pediatric US Open-Label

Phase I Pediatric Open-Label

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Report an Adverse Event or Quality Complaint

Call 1-844-MED-MLNT
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You may also report suspected
adverse events to the FDA
at 1-800-FDA-1088 or
https://www.fda.gov/medwatch
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“AE”

Report an Adverse Event
or Quality Complaint

Call 1-844-MED-MLNT
(+1 844-633-6568)
.
You may also report suspected
adverse events to the FDA
at 1-800-FDA-1088 or
https://www.fda.gov/medwatch
“QR”

CallB

1-844-MED-MLNT
(+1 844-633-6568)
to speak with a Medical
Information Representative