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OpenTrials
Completed

NCT Number: NCT05429840

Safety & PK of Single Doses of MT1980

MT1980 is being developed as a treatment for neuroinflammation (an inflammatory response in the brain and/or spinal cord). Much research has focused on the central role of neuroinflammation in the pathogenesis of many conditions relating to the CNS, including eg, traumatic brain injury, stroke, Alzheimer's disease, post-operative cognitive decline (POCD)/perioperative neurocognitive disorder, and now even long-term cognitive side effects from severe acute respiratory syndrome corona virus 2 (SARS-CoV-2). Current anti-inflammatories do not easily cross the blood-brain barrier from the systemic circulation to the brain, making neuroinflammation a difficult condition to treat.

This will be a Phase 1, single dose, randomized, placebo-controlled study in healthy subjects. The study will provide information on the safety of MT1980, the systemic bioavailability of the active drug, and levels of the active drug in the CSF. The study will be conducted in two parts. In Part 1, subjects will be randomized to receive a single oral dose of MT1980 or placebo in a parallel design. An interim PK and safety data analysis will be performed after Part 1 prior to dose selection in Part 2. In Part 2 subjects will be randomized to receive either placebo or a single oral dose of MT1980 at one of 2 strengths in a parallel design.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Icon Early Development Services

Groningen, Netherlands

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy volunteers with good physical and mental health
  • Body Mass Index 18 to 30 kg/m2
  • Men & women of child-bearing potential must agree to use adequate contraception
  • Willing & able to provide written informed consent and to communicate and participate in the study

Exclusion criteria

  • Clinically significant abnormal biochemistry, haematology, urinalysis results
  • Results of screening liver function or kidney function tests outside of normal ranges
  • Heavy daily smoking or use of nicotine containing substances

Treatment and study plan

MT1980

Drug

single dose

Placebo

Drug

single dose

Primary outcomes

  1. Treatment-related adverse events

    Time frame: Day 1 to Day 11

    Descriptive statistics comparing MT1980 & placebo following a single dose of study drug. Number of subjects, number of events and severity of events to be reported

Secondary outcomes

  1. Systemic bioavailability of MT1980

    Time frame: 72 hours post dose

  2. Level of MT1980 in CSF

    Time frame: up to 7 hours post dose

Sponsors and collaborators

Lead sponsor

Monument Therapeutics Limited

Industry

Collaborators

  • ICON plc

Registry information

Official study title

A Two-part, Single Dose, Randomized, Single Blinded, Placebo Controlled, Phase I Study to Assess the Safety and Pharmacokinetics of Oral MT1980 in Healthy Volunteers When Dosed in the Fasted State

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jun 23, 2022
Registry last updated
Nov 2, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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