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A randomized, double-blind, placebo-controlled, single ascending dose study to examine the safety, tolerability and pharmacokinetics of orally administered PHA-022121 in healthy subjects.

A randomized, double-blind, placebo-controlled, single ascending dose study to examine the safety, tolerability and pharmacokinetics of orally administered PHA-022121 in healthy subjects. - CS0348-200190 Pharvaris SAD

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON49665
Enrollment
32
Registered
2020-04-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hereditary Angioedema (HAE)

Interventions

Sponsors

Pharvaris B.V.
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Healthy male and female subjects of non-childbearing potential. Between 18 and 65 years of age, inclusive. Body mass index (BMI) between 18.0 and 30.0 kg/m2 (inclusive). Healthy on the basis of physical examination, medical history, vital signs, clinical laboratory tests, and 12-lead ECG performed at screening. If any of the results are abnormal, the subject may be included only if the investigator judges that the abnormalities or deviations from normal are not clinically significant. This determination must be recorded in the subject's source documents and initialled by the investigator. A resting heart/pulse rate (supine position for 5 minutes) between 40 and 100 beats per minute (bpm). If heart/pulse rate is out of range, up to 2 repeated assessments are permitted. A resting blood pressure (supine position for 5 minutes) between 90 and 140 mmHg systolic, inclusive, and between 40 to 90 mmHg diastolic. If blood pressure requirements are out of range, up to 2 repeated assessments are permitted.

Exclusion criteria

Exclusion criteria: Clinically relevant allergy (except for untreated, asymptomatic, seasonal allergies at time of dosing) or drug hypersensitivity. Known hypersensitivity to the drug substance, or any inactive ingredient(s) of the investigational product (refer to investigator's brochure). History of any medical condition or prior surgery of the GI-tract that could alter the absorption of orally administered drugs (does not apply to history of appendectomy). History or current evidence of any form of angioedema. History or current evidence of any form of bronchial asthma.

Design outcomes

Primary

MeasureTime frame
Primary Endpoints: Primary endpoint, safety: All standard safety assessments including physical examination, vital signs, adverse events, hematology, chemistry, urinalysis and ECG. Primary endpoint, pharmacokinetics: Plasma PK parameters tmax, Cmax, AUC0-12h, AUC0-24h, AUClast, AUCinf, t1/2, CL/F and Vz/F of PHA-022121.

Secondary

MeasureTime frame
Plasma PK parameters tmax, Cmax, AUC0-12h, AUC0-24h, AUClast, AUCinf, and t1/2, of the major metabolite M2-D. QT, and the heart rate-corrected QT interval by Fridericia*s formula (QTcF)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)