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Febrile Urinary Tract InfectionPhase 4PIVOTNCT07236944

Pivmecillinam as Oral Step-Down Treatment for Escherichia Coli Febrile Urinary Tract Infection Versus Standard of Care

A Phase 4 study testing Pivmecillinam in people with Febrile Urinary Tract Infection, run by Uppsala University at 13 sites in 2 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this clinical trial is to learn if oral treatment with pivmecillinam is effective to treat febrile urinary tract infections in adult patients. Hospitalized patients who have received 2-4 days of intravenous antibiotic therapy for febrile urinary tract infections, and have responded to treatment, will be… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Febrile Urinary Tract Infection
What is being tested?
Pivmecillinam
Could I receive a placebo?
No, everyone receives an active treatment
How many people
560 participants
Where
13 sitesin 2 countries
Study dates
Dec 2025to Mar 2029
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • ≥18 years of age.
  • Diagnosis of fUTI, defined as i) fever ≥ 38°C and ii) at least one of the following: flank pain or pelvic pain, nausea or vomiting, dysuria, urinary frequency or urgency, and costovertebral angle tenderness on physical examination.
  • Growth of E. coli in urine with antimicrobial susceptibility to mecillinam.
  • Adequate intravenous antibiotic treatment for fUTI (defined below) for 2 days to which the isolated E. coli is determined susceptible.
  • Defervescence and hemodynamic stability for at least 24 hours, according to the responsible physician.
  • Planned treatment with one of the following antibiotics, should the patient be randomized to the standard-of-care arm. Intravenous antibiotics: 1) Penicillins; ampicillin, piperacillin/tazobactam, ≥2) cephalosporins; cefotaxime, cefuroxime, ceftriaxone, 3) carbapenems; ertapenem, imipenem, meropenem, 4) monobactams; aztreonam, 5) aminoglycosides; amikacin, gentamicin, tobramycin, 6) other; fosfomycin. Oral antibiotics: 1) ciprofloxacin, 2) trimethoprim-sulfamethoxazole, 3) amoxicillin or amoxicillin/clavulanic acid provided that the isolated E. coli is determined susceptible according to the EUCAST-breakpoint for systemic infections, i.e., MIC ≤ 8 mg/l, and high dosing is used (≥750 mg amoxicillin x 3 and ≥750 mg amoxicillin/125 mg clavulanic acid x 3, respectively) and 4) tebipenem (if approved by the EMA).
  • Signed informed consent.

Who cannot join

  • Adequate intravenous antibiotic treatment for > 4 days prior to randomization or other adequate (microbiologically active) oral antibiotic treatment for the same fUTI episode prior to recruitment.
  • Growth of other bacterial species than E. coli, or fungi, in urine.
  • Contraindication for pivmecillinam (e.g. allergy).
  • Clinical suspicion of bacterial prostatitis.
  • Renal abscess.
  • Kidney transplant.
Show all 17Show fewer
  • Myelosuppressive disorder with neutrophil count < 0.5 x 10(9)/L at randomization.
  • Planned antibiotic treatment for fUTI > 14 days.
  • Likely to be prescribed antibiotic prophylaxis after treatment.
  • Other intravenous or oral antibiotic treatment; ongoing or planned during the follow-up period (i.e. until 28 days after EOT for fUTI).
  • Severe renal impairment (eGFR < 20 mL/min) at randomization.
  • Morbid obesity (BMI > 40 kg/m2).
  • Pregnancy or breastfeeding.
  • Unlikely to follow instructions or the study protocol.
  • Previous participation in the study.
  • If consenting to microbiome analysis: i) contraindication for ciprofloxacin (e.g. allergy), ii) unlikely to be able to provide fecal samples per protocol, iii) treatment with antibiotics in the past 3 months before the current fUTI episode, iv) chronic intestinal disease or previous surgery in the gastrointestinal tract.
  • If consenting to pharmacokinetic analysis: expected difficulties in providing blood and urine samples per protocol.

Trial locations and contacts

13 sites in 2 countries. Contact the study team or a site near you to ask about taking part.

Thomas Tängdén, MD, Professor contact

+46 708 370323

thomas.tangden@medsci.uu.se

Lisa Faxén, MD, PhD student contact

+46 768 721806

lisa.faxen@medsci.uu.se

13 sites in 2 countries

Sweden11 sites, 11 recruiting
  • Södra Älvsborg Hospital

    Borås

    Anders Lundqvist, MD, PhD, anders.lundqvist@vgregion.se

    Not yet recruiting
  • Eskilstuna Hospital

    Eskilstuna

    Joakim Lundvik, MD, joakim.lundvik@regionsormland.se

    Not yet recruiting
  • Sahlgrenska University Hospital

    Gothenburg

    Erik Sörstedt, MD, PhD, erik.sorstedt@vgregion.se

    Hanna Montelin, MD, PhD, hanna.montelin@medsci.uu.se

    Recruiting
  • Blekinge Hospital

    Karlskrona

    Eva Lindqvist, MD, eva.lindqvist@regionblekinge.se

    Not yet recruiting
  • Skåne University Hospital

    Lund

    Christian Kampmann, MD, PhD, christian.kampmann@skane.se

    Not yet recruiting
  • Örebro University Hospital

    Örebro

    Edvin Ingberg, MD, PhD, edvin.ingberg@regionorebrolan.se

    Recruiting
  • Karolinska University Hospital

    Stockholm

    Pontus Nauclér, MD, Professor, pontus.naucler@ki.se

    Not yet recruiting
  • Sundsvall Hospital

    Sundsvall

    Björn Diedrichs, MD, bjorn.diedrichs@rvn.se

    Not yet recruiting
  • Umeå University Hospital

    Umeå

    Urban Johansson Kostenniemi, MD, PhD, urban.johansson.kostenniemi@regionvasterbotten.se

    Not yet recruiting
  • Uppsala University Hospital

    Uppsala

    Thomas Tängdén, MD, Professor, + 46 708370323, thomas.tangden@medsci.uu.se

    Lisa Faxén, MD, PhD student, +46 768 72 18 06, lisa.faxen@medsci.uu.se

    Recruiting
  • Central Hospital Växjö

    Vaxjo

    Olof Elvstam, MD, PhD, olof.elvstam@med.lu.se

    Not yet recruiting

Other trials in Sweden

Norway2 sites, 2 recruiting
  • Haukeland University Hospital

    Haukeland

    Eivind Rath, MD, PhD, eivind.rath@helse-bergen.no

    Not yet recruiting
  • Oslo University Hospital

    Oslo

    Kristian Tonby, MD, Associate professor, kritonby@ous-hf.no

    Not yet recruiting

Other trials in Norway

About this study

Official title: Pivmecillinam as Oral Step-Down Treatment for Escherichia Coli Febrile Urinary Tract Infection Versus Standard of Care: A Randomized Controlled Non-Inferiority Multicenter Trial

The goal of this clinical trial is to learn if oral treatment with pivmecillinam is effective to treat febrile urinary tract infections in adult patients. Hospitalized patients who have received 2-4 days of intravenous antibiotic therapy for febrile urinary tract infections, and have responded to treatment, will be randomized to either pivmecillinam or standard treatment (other oral or intravenous antibiotics).

The main question the study aims to answer is if oral follow-up with pivmecillinam is as effective as standard treatment. Patients will be evaluated for clinical response (resolution of fever and urinary tract symptoms) and microbiological response (no growth of bacteria in urine) 7 and 28 days after the end of treatment. Patients will also be asked about side effects. Some of the participants will also be examined for changes in the gut microbiome and drug exposures in blood and urine.

Read more

Participants will:

  1. Keep a patient diary to record antibiotic intake, body temperature, urinary tract symptoms, and suspected side effects until 7 days after end of treatment.
  2. Participate in phone interviews 7 and 28 days after end of treatment to assess clinical response.
  3. Provide urine samples 7 and 28 days after end of treatment to evaluate microbiological response.
  4. A subgroup (60 patients) will provide fecal samples at five time-points over three months to assess antibiotic-induced changes in the gut microbiome.
  5. A subgroup (30 patients) treated with to pivmecillinam will provide blood and urine samples to determine the pharmacokinetics of mecillinam during one dosing interval.
Read the detailed description

Background:

Escherichia coli is the predominant uropathogen and the most common cause of bloodstream infections. In the hospital setting, patients with febrile UTI (fUTI) are normally treated with intravenous antibiotics for 2-4 days until clinical improvement followed by oral step-down treatment guided by microbiological antibiotic susceptibility testing results. However, oral treatment options are increasingly limited due to emerging resistance in uropathogens and the lack of new antibiotics.

This non-inferiority, open label, randomized clinical trial (RCT), conducted in Sweden and Norway, will evaluate the efficacy of an oral narrow-spectrum penicillin (pivmecillinam) as oral step-down for patients with fUTI caused by Escherichia coli. Pivmecillinam is a first line antibiotic for acute cystitis and is sometimes used also for fUTI in Denmark and Norway although no previous RCT has evaluated its efficacy for this indication. Pivmecillinam will be compared to standard of care, i.e. step-down treatment with other orally administered antibiotics, such as ciprofloxacin or trimethoprim-sulfamethoxazole, or continued intravenous antibiotic treatment. The target sample size is 560 participants, to be enrolled over a three-year period.

Patient population:

The following PICO (Population/Intervention/Control/Outcome) applies: Population - Patients with E. coli fUTI receiving initial intravenous antibiotic treatment; Intervention - Oral follow-up treatment with pivmecillinam; Control - Standard of care; Outcome - Clinical response (primary endpoint).

Objectives:

The primary objective is to investigate if the clinical response with oral follow-up treatment with pivmecillinam 400 mg four times a day (QID) is non-inferior to standard of care in patients with E. coli fUTI 7 (+/-2) days after end of treatment (EOT).

Secondary objectives are to investigate treatment effects on:

  1. Sustained clinical response 28 days after EOT
  2. Microbiological response 7 days after EOT
  3. Sustained microbiological response 28 days after EOT
  4. Adverse events up to 7 days after EOT
  5. Disturbances in the intestinal microbiome (60 patients) up to 3 months after EOT
  6. Pharmacokinetics of mecillinam in plasma and urine (30 patients) during one dosing interval
  7. Cost effectiveness of pivmecillinam compared to standard treatment

Primary endpoint:

The primary endpoint is defined as clinical response, defined as: i) no new healthcare contacts or antibiotic treatments for suspected or proven UTI, ii) sustained defervescence (< 38°C), and iii) patient-documented resolution of fUTI symptoms that were present and recorded in the eCRF at trial entry (and no new fUTI symptoms) at test of cure (TOC), which will be performed 7 (+/-2) days after EOT. The evaluation of clinical response (primary endpoint) will be performed by blinded assessors.

Statistical analysis:

Non-inferiority will be defined as < 10% lower clinical response at TOC. The primary analysis will be based on all randomized patients (intention-to-treat, ITT). Per-protocol (PP) analysis will be performed as supplementary analysis, and the consistency of ITT and PP results will be evaluated. Assuming 80% clinical response rate in both arms, a non-inferiority limit of 10%-points, 1:1 randomization, and 10% loss to follow-up, 280 patients in each arm (total 560 randomized patients) would give 80% power to detect non-inferiority at a one-sided alpha=0.025.

Intervention and control group:

Patients with fUTI caused by E. coli treated with adequate intravenous antibiotics for 2-4 days will be randomized to i) oral step-down treatment with pivmecillinam (high dose, 400 mg QID), or ii) standard of care. Patients randomized to pivmecillinam will be provided with tablets for a total treatment duration of 7 (female patients with no complicating factors) or 10 days (all other patients).

The control group will receive standard treatment, as determined by the responsible physician in accordance with current treatment guidelines and guided by the antibiotic susceptibility testing results of the isolated pathogen. The total treatment duration will be 7 to 14 days. In Norway, where pivmecillinam is already recommended for some patients with fUTI, participants randomized to the control group can be prescribed any antibiotic considered standard of care except for pivmecillinam. The following antibiotics will be considered adequate if the isolated bacteria are reported susceptible to the prescribed drug by the clinical microbiological laboratory. Intravenous antibiotics: 1) Penicillins; ampicillin, piperacillin/tazobactam, 2) cephalosporins; cefotaxime, cefuroxime, ceftriaxone, 3) carbapenems; ertapenem, imipenem, meropenem, 4) monobactams; aztreonam, 5) aminoglycosides; amikacin, gentamicin, tobramycin, 6) other; fosfomycin. Oral antibiotics: 1) ciprofloxacin, 2) trimethoprim-sulfamethoxazole, 3) amoxicillin or amoxicillin/clavulanic acid provided that the isolated E. coli is determined susceptible according to the EUCAST breakpoint for systemic infections, i.e., MIC ≤ 8 mg/l, and high dosing is used (≥750 mg amoxicillin x 3 and ≥750 mg amoxicillin/125 mg clavulanic acid x 3, respectively) and 4) tebipenem (if approved by the EMA).

Diagnostic and monitoring procedures:

TOC will be performed 7 (+/- 2) days after EOT by phone interview. A second follow-up will be performed 28 (+/- 2) days after EOT to assess sustainable clinical response. Urine samples will be collected 7 and 28 days after EOT to evaluate microbiological response.

Fecal samples for microbiome analysis will be collected from 30 patients treated with pivmecillinam and 30 patients treated with ciprofloxacin at the time of randomization (prior to oral treatment), at EOT, and 7 days, 28 days, and 3 months after EOT (±2 days).

The pharmacokinetics of mecillinam in plasma and urine will be assessed in 30 patients treated with pivmecillinam. Blood samples will be drawn in conjunction with the third dose or later, at 0 h (before dose), and 1 h, 2 h, 4 h and 6 h (after dose). Urine sampling will be performed within one dosing interval after ≥3 doses during 0-3 h and 3-6 h.

Risk/benefit assessment:

Pivmecillinam is commonly used and proven safe for uncomplicated cystitis, and the risks of study participants is considered very low. If pivmecillinam shows non-inferiority to standard of care, the results of the study will benefit patients with fUTI as well as health care and society at large. A shift to oral treatment means shorter hospitalization and no need for repeated visits or intravenous catheters, thereby reducing suffering, the risk of healthcare-associated infections, and costs. Using a narrow-spectrum antibiotic instead of broad-spectrum antibiotics reduces the risks of side effects and emergence and spread of resistant bacteria. The study will also provide a better understanding of the relative collateral damage of the study drugs on the microbiome and pivmecillinam pharmacokinetics, which will inform future treatment decisions and dosing.

Being tested
Pivmecillinam, Standard of Care (Investigator Choice)
Keywords
Urinary Tract Infection, Pivmecillinam, Escherichia coli
Medical subject headings
Urinary Tract Infections, Escherichia coli Infections

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PivmecillinamDrug

    Patients randomized to pivmecillinam will be provided with 400 mg tablets for 3 to 8 days of treatment, to be taken four times daily, resulting in a total treatment duration of 7 or 10 days (including the initial 2-4 days of intravenous treatment). The shorter treatment duration of 7 days will be used for female patients with no complicating factors (structural or functional urologic abnormalities, urinary tract catheterization, and diabetes mellitus). The longer treatment duration of 10 days will be used for all other patients.

  • Standard of Care (Investigator Choice)Drug

    The control group will receive standard of care antibiotic treatment at the discretion of the responsible physician and according to existing treatment guidelines, with a total treatment duration of 7 to 14 days. The following antibiotics will be considered adequate. Intravenous antibiotics: 1) Penicillins; ampicillin, piperacillin/tazobactam, 2) cephalosporins; cefotaxime, cefuroxime, ceftriaxone, 3) carbapenems; ertapenem, imipenem, meropenem, 4) monobactams; aztreonam, 5) aminoglycosides; amikacin, gentamicin, tobramycin, 6) other; fosfomycin. Oral antibiotics: 1) ciprofloxacin, 2) trimethoprim-sulfamethoxazole, 3) amoxicillin or amoxicillin/clavulanic acid provided that the isolated E. coli is determined susceptible according to the EUCAST-breakpoint for systemic infections, i.e., MIC ≤ 8 mg/l, and high dosing is used (≥750 mg amoxicillin x 3 and ≥750 mg amoxicillin/125 mg clavulanic acid x 3, respectively) and 4) tebipenem (if approved by the EMA).

Study groups in NCT07236944
Study groupRoleWhat they receive
Standard of careActive comparatorThe control group will receive standard of care treatment at the discretion of the responsible physician and according to existing treatment guidelines.
Receives: Drug: Standard of Care (Investigator Choice)
PivmecillinamExperimentalPivmecillinam (high dose, 400 mg four times daily).
Receives: Drug: Pivmecillinam

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Clinical response (primary endpoint).

    Clinical response: i) no new healthcare contacts or antibiotic treatments for suspected or proven UTI, ii) sustained defervescence (< 38°C), and iii) patient-documented resolution of fUTI symptoms that were present and recorded in the eCRF at trial entry (and no new fUTI symptoms) at test of cure (TOC), which will be performed 7 (+/-2) days after end of treatment (EOT).

    The evaluation of clinical response (primary endpoint) will be performed by blinded assessors.

    Measured: 7 (+/-2) days after EOT

Secondary outcomes (4)
  1. Sustained clinical response

    Sustained clinical response: i) no new healthcare contacts or antibiotic treatments for suspected or proven UTI, ii) no recurrent fever (≥ 38°C), and iii) no recurrent UTI symptoms after completion of the initial therapy and until 28 (+/- 2) days after EOT.

    Measured: 28 (+/- 2) days after EOT

  2. Microbiological response

    Microbiological response: no detectable growth of E. coli in urine sampled at TOC, i.e., 7 (+/-2) days after EOT.

    Measured: 7 (+/-2) days after EOT

  3. Sustained microbiological response

    Sustained microbiological response: no detectable growth of E. coli in urine sampled at the second follow-up 28 (+/- 2) days after EOT.

    Measured: 28 (+/- 2) days after EOT

  4. Occurrence and severity of adverse events

    Occurrence and severity of adverse events from start of study treatment until TOC; recorded by the participants in a study diary, documented in the medical records, or reported at the TOC follow-up.

    Measured: From start of study treatment until test of cure 7 (+/-2) days after EOT

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Nov 2025
  2. Study startDec 2025 (estimated)
  3. Primary completionMar 2029 (estimated)
  4. Study completionMar 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
560 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07236944
Sponsor's protocol ID
PIVOT
Other IDs
2023-503447-33-00, 2023
Acronym
PIVOT
Status last verified
Nov 2025
First submitted
14 Nov 2025
Last updated
17 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Pivmecillinam in people with Febrile Urinary Tract Infection, run by Uppsala University at 13 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 17 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 13 sites in Sweden, Norway. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Thomas Tängdén, MD, Professor (+46 708 370323, thomas.tangden@medsci.uu.se), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Clinical response (primary endpoint). (time frame: 7 (+/-2) days after EOT). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Dec 2025.

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