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Completed

NCT Number: NCT07055321

A Phase 1, First-in-human Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Doses of ETH47 in Healthy Participants

This first-in-human study is designed to evaluate the safety, tolerability, pharmacokinetics and target engagement of ETH47 in healthy participants following single intranasal and single inhaled administration

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

CRO

Merthyr Tydfil, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF), restriction handbook and in this protocol.
  • Participants who are overtly healthy, as determined by screening assessments and the Investigator's judgement, aged ≥18 and ≤55 years at the time of obtaining informed consent.
  • Body mass index of 18.5 to 32 kg/m2 (inclusive).
  • Participants must agree to use contraception methods.
  • Parts B only: participants must be able to perform reliable and reproducible pulmonary function tests and meet the following criteria at screening:
  • Forced expiratory volume in one second (FEV1) ≥80 % predicted by third National Health and Nutrition Examination Survey standards, and
  • Change in FEV1 and forced vital capacity <200 mL, 15 minutes after 4 puffs of inhaled short-acting beta 2-agonists.

Major Exclusion Criteria:

  • History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, neuropsychiatric, autoimmune, or immunosuppressive disorders which, in the Investigator's judgement, puts the participant at risk due to participation in the trial, may influence the results of the trial, or the subject's ability to participate in the trial.
  • Signs or symptoms of upper or lower respiratory tract infection within 2 weeks of randomisation.
  • Participants who are SARS-CoV-2 positive.
  • Known or positive laboratory results at screening for human immunodeficiency virus (HIV) infection, hepatitis B or hepatitis C.
  • Any malignancy except for the following:
  • Adequately treated basal cell carcinoma or
  • History of any other cancer where the disease-free period is ≥5 years.
  • The evidence of any other active or chronic disease following a detailed medical and surgical history, a complete physical examination including vital signs, haematology, blood chemistry, serology, and urinalysis.

Treatment and study plan

ETH47

Drug

Dose level 1; single intranasal administration

Primary outcomes

  1. Number of treatment-emergent adverse events (TEAEs)

    Time frame: From treatment until end of study (d 21)

  2. Number of serious adverse events (SAEs)

    Time frame: From enrollment until end of study (day 21)

Sponsors and collaborators

Lead sponsor

Ethris GmbH

Industry

Registry information

Official study title

A Phase 1, First-in-human, Randomized, Participant- and Investigator-blinded, Placebo-controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Doses of ETH47 in Healthy Participants

Acronym: ETH47-101

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jul 8, 2025
Registry last updated
Jul 8, 2025

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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