Efficacy of Combination Baloxovir and Oseltamivir Therapy in Influenza Infected Immunocompromised Hosts

Who is this study for? Patients with Hematopoietic and Lymphoid Cell Neoplasm, Influenza
What treatments are being studied? Oseltamivir
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This phase II trial studies the effect of baloxavir in combination with oseltamivir in treating severe influenza infection in patients who have previously received a hematopoietic (blood) stem cell transplant or have a hematological malignancy. Baloxavir is an antiviral drug that inhibits the growth of influenza virus, reduces viral load and prevents further influenza infection. Osetamivir is an antiviral drug that blocks enzymes on the surfaces of influenza viruses, interfering with cell release of complete viral particles. Giving baloxavir in combination with oseltamivir may shorten or decrease the intensity of influenza infection compared to oseltamivir alone.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Healthy Volunteers: f
View:

• Hematopoeitic cell transplant recipients OR hematological malignancy patients

• Diagnosed with influenza ⱡ

• Evidence of LRTI\* or high risk upper respiratory tract infection (URTI)\*\*

⁃ ⱡ A positive multiplex PCR for influenza is required to confirm a diagnosis of influenza infection.

⁃ \* LRTI will be defined as influenza cases that have evidence of disease below the level of the trachea on either imaging only (possible LRTI), imaging and microbiological evidence of lower airway disease with a bronchoscopy (probable LRTD) or pathological evidence of disease via biopsy (proven LRTI).

⁃ \*\* High risk URI will be defined as those cases of influenza that do not have microbiological nor radiological evidence of LRTI, yet they have an immunodeficiency scoring index (ISI) of 3 or greater as defined by Shah D et al (19) for HCT recipients or severe neutropenia (ANC ≤500 cells/ml) and/or lymphopenia (ALC ≤200 cells/ml) for HM patients.

Locations
United States
Texas
M D Anderson Cancer Center
RECRUITING
Houston
Contact Information
Primary
Roy F. Chemaly, MD,MPH
rfchemaly@mdanderson.org
713-792-6830
Time Frame
Start Date: 2021-10-11
Estimated Completion Date: 2028-02-28
Participants
Target number of participants: 60
Treatments
Experimental: Arm I (oseltamivir, baloxavir marboxil)
Patients receive oseltamivir PO BID for up to 10 days and baloxavir marboxil PO every 72 hours for a total of 3 doses in the absence of disease progression or unacceptable toxicity.
Active_comparator: Arm II (oseltamivir)
Patients receive oseltamivir PO BID for up to 10 days in the absence of disease progression or unacceptable toxicity.
Related Therapeutic Areas
Sponsors
Leads: M.D. Anderson Cancer Center

This content was sourced from clinicaltrials.gov