Prospective Evaluation of Xerava Prophylaxis in Hematological Malignancy Patients With Prolonged Neutropenia
Recruiting
Phase 2
Interventional Study
Hematological Malignancy
Neutropenia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Trial phase
- Phase 2
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 55 (estimated)
- Sponsor
- West Virginia University · Other
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About This Trial
Antibacterial prophylaxis is recommended in patients at high risk of infection, specifically patients undergoing acute leukemia induction therapy or hematopoietic stem cell transplant (HSCT) who are expected to have profound neutropenia (ANC\<100 neutrophils/milliliter) for more than seven days. Xerava™ (eravacycline) has a broad spectrum of activity including many multi-drug resistant strains of …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* All patients receiving induction chemotherapy for treatment of acute leukemia or receiving preparative regimen for HSCT
* Patient must provide informed consent.
* Bilirubin ≤ 3 x the ULN and AST/ALT ≤ 5 x ULN
Exclusion Criteria:
* Uncontrolled bacterial, viral or fungal infe…
Contacts