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COMPLETED Phase 2

Study of the Safety, Tolerability, and Pharmacokinetics of LHW090 in Patients With Moderately Impaired Renal Function

NCT02678000 · View on ClinicalTrials.gov ↗

Study Summary

This was a randomized, double-blind, parallel group, placebo-controlled study, in two sequential parts that evaluated the renal safety, tolerability and pharmacokinetics of LHW090 in patients with moderately impaired renal function.

Interventions

  • DRUG Placebo
  • DRUG LHW090

Study Locations (12)

Other

  • Novartis Investigative Site — Berlin
  • Novartis Investigative Site — Elsterwerda
  • Novartis Investigative Site — Erlangen
  • Novartis Investigative Site — Hamburg
  • Novartis Investigative Site — Mannheim

Florida

  • Novartis Investigative Site — Miami Lakes
  • Novartis Investigative Site — Orlando

Minnesota

  • Novartis Investigative Site — Minneapolis
  • Novartis Investigative Site — Saint Paul

California

  • Novartis Investigative Site — Anaheim

Colorado

  • Novartis Investigative Site — Lakewood

Louisiana

  • Novartis Investigative Site — New Orleans

Trial Details

FieldValue
Enrollment Target 84 participants
Start Date 2017-03-10
Est. Completion 2018-10-11
Phase Phase 2

Sponsor

Novartis Pharmaceuticals

792 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02678000

The ClinicalTrials.gov registry entry for NCT02678000 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 84 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis Pharmaceuticals, which has 792 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Chronic Kidney Disease (CKD) appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02678000 reports 12 study locations spanning 6 distinct geographic areas — top geographies include Other, Florida, Minnesota. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02678000 about?

NCT02678000 is a clinical study titled "Study of the Safety, Tolerability, and Pharmacokinetics of LHW090 in Patients With Moderately Impaired Renal Function". This was a randomized, double-blind, parallel group, placebo-controlled study, in two sequential parts that evaluated the renal safety, tolerability and pharmacokinetics of LHW090 in patients with moderately impaired renal function.

What is the current status of trial NCT02678000?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 84 participants. The study started on 2017-03-10. Estimated completion is 2018-10-11.

What conditions does trial NCT02678000 study?

This clinical trial studies the following conditions: Chronic Kidney Disease (CKD). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02678000?

The interventions under investigation include: Placebo (DRUG), LHW090 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02678000?

This trial is sponsored by Novartis Pharmaceuticals, which has 792 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02678000 being conducted?

This trial has 12 study locations across California, Colorado, Florida, Louisiana, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial