findmyKOL
Clinical trialNCT03788967CompletedPhase 3Interventional

Study to Assess the Efficacy, Safety and Pharmacokinetics of Orally Administered Tebipenem Pivoxil Hydrobromide (SPR994) Compared to Intravenous Ertapenem in Participants With Complicated Urinary Tract Infection (cUTI) or Acute Pyelonephritis (AP)

SponsorSpero TherapeuticsEnrollment1,372Acute PyelonephritisComplicated Urinary Tract Infection
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

96 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Bulgaria
  • Medical Facility

    Blagoevgrad, Bulgaria

  • Medical Facility

    Dobrich, Bulgaria

  • Medical Facility

    Rousse, Bulgaria

  • Medical Facility

    Shumen, Bulgaria

  • Medical Facility

    Sofia, Bulgaria

  • Medical Facility

    Sofia, Bulgaria

  • Medical Facility

    Veliko Tarnovo, Bulgaria

Czechia
  • Medical Facility

    Karlovy Vary, Czechia

  • Medical Facility

    Liberec, Czechia

  • Medical Facility

    Prague, Czechia

  • Medical Facility

    Zlín, Czechia

  • Medical Facility

    Ústí nad Labem, Czechia

Estonia
  • Medical Facility

    Kohtla-Järve, Estonia

  • Medical Facility

    Tallinn, Estonia

  • Medical Facility

    Võru, Estonia

Georgia
  • Medical Facility

    Tbilisi, Georgia

  • Medical Facility

    Tbilisi, Georgia

  • Medical Facility

    Tbilisi, Georgia

  • Medical Facility

    Tbilisi, Georgia

  • Medical Facility

    Zestaponi, Georgia

Hungary
  • Medical Facility

    Budapest, Hungary

  • Medical Facility

    Budapest, Hungary

  • Medical Facility

    Nagykanizsa, Hungary

  • Medical Facility

    Nyíregyháza, Hungary

  • Medical Facility

    Tatabánya, Hungary

Latvia
  • Medical Facility

    Riga, Latvia

  • Medical Facility

    Riga, Latvia

  • Medical Facility

    Valmiera, Latvia

Moldova
  • Medical Facility

    Chisinau, Moldova

  • Medical Facility

    Chisinau, Moldova

Poland
  • Medical Facility

    Katowice, Poland

  • Medical Facility

    Krakow, Poland

  • Medical Facility

    Lodz, Poland

  • Medical Facility

    Oświęcim, Poland

  • Medical Facility

    Wroclaw, Poland

Romania
  • Medical Facility

    Bucharest, Romania

  • Medical Facility

    Bucharest, Romania

  • Medical Facility

    Bucharest, Romania

  • Medical Facility

    Craiova, Romania

  • Medical Facility

    Iași, Romania

56 more sites on the registry record.ClinicalTrials.gov ↗

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
3 Jun 2019
Primary completion
20 May 2020
Completion
27 May 2020
Last update posted
25 Jul 2022
Registered enrollment
1,372
Registry id
NCT03788967

Cross-registrations

EU-CTR / CTIS (EudraCT)2018-003671-35

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.