An fMRI Study in Healthy Volunteers to Investigate the Effects of ABX-1431 on Experimental Hyperalgesia and Its Neural Correlates

• Status: Completed
• Trial end date: 2018-03-01
• Target enrollment: 0
• Participant gender: Male

Summary

An fMRI study in healthy volunteers to investigate the effects of ABX-1431 on experimental hyperalgesia and its neural correlates.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Abide Therapeutics
• Collaborator: University of Oxford

Criteria

Inclusion Criteria:

• Understands the study procedures and is willing and able to give informed consent for participation in the trial.

• Male, right-handed, aged 18 to 55 years of age at the first visit.

• Body mass index >18 and ≤30 kg/m2 at the first visit.

• Judged to be in good health based on medical history, physical examination, vital sign measurements, and laboratory safety tests (see appendix A for interpretation of laboratory findings) obtained at the first visit.

• No clinically significant abnormality of ECG performed on the first visit.

• Is a non-smoker and has not used nicotine or nicotine-containing products for at least 3 months.

• In the Investigator's opinion, participant is able and willing to comply with all trial requirements.

• Willing to allow his or her General Practitioner to be notified of participation in the trial and to confirm the eligibility of the participant.

• Able to tolerate MRI scanning at the first visit. Responds to topical capsaicin by attaining a pain score of at least 4/10, assessed on the first visit.

Exclusion Criteria:

• A current acute pain condition.

• A personal history of a chronic pain condition.

• Contraindications to MRI scanning.

• Scheduled elective surgery or other procedures requiring general anesthesia during the trial.

• A personal history of a clinically significant psychiatric disorder (including severe affective disorder, anxiety disorders, psychotic tendencies and drug-induced psychoses). Subjects who have had situational depression in the past may be enrolled at the discretion of the investigator.

• A first-degree family history of schizophrenia, major affective disorder, or other psychosis.

• Participant is mentally or legally incapacitated, has significant emotional problems at the time of the first visit, or is expected to have potential for mental incapacitation during the conduct of the study.

• A history of any illness that, in the opinion of the investigator, might confound the results of the study or pose an additional risk to the participant by virtue of their participation in the study.

• An estimated creatinine clearance of ≤80ml/min based on the Cockcroft-Gault equation. An actual creatinine clearance, as measured using a 24-hour urine collection, may be used in place of, or in conjunction with the Cockcraft-Gault calculation. Subjects with an actual or calculated creatinine clearance that is in the range of 72-79 mL/min (i.e., within 10% of 80 mL/min) may be enrolled in the study at the discretion of the Investigator.

• A history of stroke, chronic seizures, or major neurological disorder.

• A history of clinically significant (in the opinion of the investigator) endocrine, gastrointestinal, cardiovascular, peripheral vascular, hematological, hepatic, immunological, renal, respiratory, or genitourinary abnormalities or diseases. Participants with history of uncomplicated kidney stones (defined as spontaneous passage and no recurrence in the last 5 years) or childhood asthma may be enrolled in the trial at the discretion of the investigator.

• A history of clinically significant neoplastic disease, with the exception of adequately treated localized or in situ non-melanoma carcinoma of the skin.

• A history of significant multiple and/or severe allergies (e.g. food, drug, latex allergy), or has had an anaphylactic reaction or significant intolerability to prescription or non-prescription drugs (including capsaicin and marijuana or other cannabis-containing drugs) or food.

• Participants who have had major surgery or have donated or lost 1 unit (approximately 500ml) of blood within 4 weeks prior to the first visit.