Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01965808 · ClinicalTrials.gov registry record · Phase 1

A Study of LY2157299 in Healthy Participants

A Phase 1 study of Healthy Volunteers, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 1
Development phase
16
Enrollment target
1
Study location

NCT01965808: Completed Phase 1 study of Healthy Volunteers, sponsored by Eli Lilly and Company.

NCT01965808 is a Phase 1 study of Healthy Volunteers that has completed, run by Eli Lilly and Company. The registered enrollment target is 16 participants, below the 482-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01965808, a Phase 1 study of Healthy Volunteers, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
16 participants
Enrollment target
1
Study location

Study Summary

Participants in this study will receive two oral doses of 150 milligram (mg) LY2157299 taken at least 4 days apart. One dose will be given without food. One dose will be given with a high fat meal. The study will evaluate the effect of a high fat meal on how much of the drug gets into the blood stream. Side effects will be documented. This study will last approximately 15 days not including screening. Screening is required within 30 days prior to the start of the study.

Conditions Studied

Interventions

  • DRUG LY2157299

Study Locations (1)

Florida

  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Daytona Beach

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2013-10
Est. Completion 2013-12
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT01965808 record still lists

NCT01965808 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 482-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Healthy Volunteers appearing as the primary indexed condition, and to 1 intervention - of which LY2157299 is the first listed.

NCT01965808 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT01965808 about?

NCT01965808 is a clinical study titled "A Study of LY2157299 in Healthy Participants". Participants in this study will receive two oral doses of 150 milligram (mg) LY2157299 taken at least 4 days apart. One dose will be given without food. One dose will be given with a high fat meal. The study will evaluate the effect of a high fat meal on how much of the drug gets into the blood stre...

What is the current status of trial NCT01965808?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2013-10. Estimated completion is 2013-12.

What conditions does trial NCT01965808 study?

This clinical trial studies the following conditions: Healthy Volunteers.

What interventions are being tested in trial NCT01965808?

The interventions under investigation include: LY2157299 (DRUG).

Who is sponsoring clinical trial NCT01965808?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01965808 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy Volunteers

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01965808's enrollment target sits among peer trials

16 235th of 283 higher than 42 of 283 other Healthy Volunteers trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy Volunteers trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02422641 · 16 participants · Phase 2

    Prospective Evaluation Of High-Dose Systemic Methotrexate In Patients With Breast Cancer And Leptomeningeal Metastasis

  • NCT02851758 · 16 participants · NA

    Transplantation of Autologously Derived Mitochondria Following Ischemia

  • NCT03291028 · 16 participants

    Analysis of Primary and Metastatic Tumors in Patients With Renal Cell Carcinoma and Urothelial Carcinoma

  • NCT03425526 · 16 participants · Phase 1

    Donor T Cell Therapy in Treating Immunocompromised Patients With Adenovirus-Related Disease

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01965808, the US trial registry maintained by the National Library of Medicine. NCT01965808 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.