# Phage Therapy for Recurrent UTIs in Kidney Transplant Recipients > **NIH NIH R01** · UNIVERSITY OF CALIFORNIA, SAN DIEGO · 2024 · $332,372 ## Abstract PROJECT SUMMARY/ ABSTRACT Recurrent urinary tract infections (rUTI) are a common problem in kidney transplant recipients (KTR), especially women, and lead to serious consequences – pyelonephritis, bacteremia, kidney dysfunction, and death. Escherichia coli and Klebsiella pneumoniae are usually implicated. Antibiotics are associated with adverse events, increased multi-drug resistance; and they do not prevent a future recurrent UTI (rUTI) due to microbiome persistence of the uropathogen. New strategies to combat rUTI are critically needed. Bacteriophage (phage) therapy consists of administration of viruses that specifically bind to target bacteria leading to an intracellular replicative lytic cell cycle causing bacterial cell death; phage therapy is currently in clinical trials for a variety of indications. Phages are highly specific to their target bacteria; this relatively narrow host range is a significant advantage that has the potential to precisely target the causative pathogen in the gut and urinary microbiome and thus remove the reservoir of rUTI. We hypothesize that phage therapy directed against E. coli and K. pneumoniae in female KTR will be safe and lead to a reduction in UTI event rate via a targeted impact on the gut and urinary microbiome. We plan to conduct a randomized phase I/II pilot clinical trial to compare the safety, tolerability, and feasibility in addition to efficacy and microbiome effects of phage therapy vs. placebo administration in asymptomatic female KTR with a history of rUTI due to E. coli or K. pnuemoniae. Participants will be randomized to receive a 7-day course of twice daily intravenous phage therapy (16 participants) or normal saline placebo (16 participants) and will be followed for 180 days for assessment of study outcomes. Primary outcome of safety and tolerability will be measured by the incidence of adverse events, abnormal vital signs and clinical laboratory tests; feasibility will be assessed with specific goals for enrollment, phage match, study drug administration, and follow-up. The main efficacy endpoint is number of UTI events due to the original infecting pathogen (E. coli, K. pneumoniae) over the 180-day study observation period (event rate), calculated for the intent to treat population. Participants will also undergo sampling (urine, stool) at baseline and during various timepoints to determine microbiome characteristics before, during, and after phage, and to establish a biospecimen repository for further hypothesis-driven research. We will use our significant expertise in kidney transplantation and UTI, unique experience with the microbiome and virome, and visionary phage therapy infrastructure to evaluate the feasibility of moving rUTI therapy in KTR towards a successful individualized approach. This research has major potential to reduce allograft injury and improve bladder health in KTR, while reducing morbidity and mortality. The results of this pilot clinical study will directly inform t... ## Key facts - **NIH application ID:** 10801997 - **Project number:** 1R01DK134726-01A1 - **Recipient organization:** UNIVERSITY OF CALIFORNIA, SAN DIEGO - **Principal Investigator:** Saima Aslam - **Activity code:** R01 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2024 - **Award amount:** $332,372 - **Award type:** 1 - **Project period:** 2024-08-16 → 2027-06-30 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10801997 ## Citation > US National Institutes of Health, RePORTER application 10801997, Phage Therapy for Recurrent UTIs in Kidney Transplant Recipients (1R01DK134726-01A1). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10801997. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*