deltatrials
Terminated PHASE1 INTERVENTIONAL 11-arm NCT03067363

First in Human Single Ascending Dose Study of MOR107

Assessment of Safety, Tolerability and Pharmacokinetics of Single Ascending Subcutaneous Doses of MOR107 in Healthy Male Subjects and Pharmacodynamics in Healthy Male Subjects on a Low Sodium Diet

Sponsor: Alan Richardson

Conditions Safety
Updated 6 times since 2017 Last updated: Feb 6, 2018 Started: Feb 16, 2017 Primary completion: Mar 23, 2017 Completion: Mar 23, 2017
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

Part 1 completed successfully. Part 2 not conducted.

A PHASE1 clinical study on Safety, this trial is terminated or withdrawn. The trial is conducted by Alan Richardson and has accumulated 6 data snapshots since 2017. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

~Apr 2017 – ~Mar 2018 · 11 months · monthly snapshotRecruiting~Mar 2018 – ~Jun 2018 · 3 months · monthly snapshotTerminated~Jun 2018 – ~Jan 2021 · 31 months · monthly snapshotTerminated~Jan 2021 – ~Jul 2024 · 42 months · monthly snapshotTerminated~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotTerminated~Sep 2024 – present · 24 months · monthly snapshotTerminated

Change History

6 versions recorded
  1. Sep 2024 — Present [monthly]

    Terminated PHASE1

  2. Jul 2024 — Sep 2024 [monthly]

    Terminated PHASE1

  3. Jan 2021 — Jul 2024 [monthly]

    Terminated PHASE1

  4. Jun 2018 — Jan 2021 [monthly]

    Terminated PHASE1

  5. Mar 2018 — Jun 2018 [monthly]

    Terminated PHASE1

    Status: RecruitingTerminated

Show 1 earlier version
  1. Apr 2017 — Mar 2018 [monthly]

    Recruiting PHASE1

    First recorded

Feb 2017

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Alan Richardson
  • Quotient Clinical
Data source: LanthioPep BV

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations