A Study to Assess Efficacy, Safety, and Tolerability of P1101 in Adult Patients With PV

Running, not enrolling · Phase 3

Conditions studied: Polycythemia Vera

In brief

A Study to Assess Efficacy, Safety, and Tolerability of P1101 in Adult Patients with PV

Key facts

Study ID: NCT05481151
Run by: PharmaEssentia
People needed: 111
Starts: 2022-10-26
Expected to finish: 2027-07-31
Last updated by the study team: 2025-08-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Male or female subjects aged ≥18 years at the time of signing the informed consent form
Subjects diagnosed with PV according to the 2008 or 2016 World Health Organization (WHO) criteria
Subjects with good liver function at screening, which is defined as total bilirubin ≤1.5 × upper limit of normal (ULN), international normalized ratio (INR) ≤1.5 × ULN, albumin >3.5 g/dL, alanine aminotransferase (ALT) ≤2.0 × ULN, and aspartate aminotransferase (AST) ≤2.0 × ULN
Hemoglobin (HGB) ≥10 g/dL for females, and HGB ≥11 g/dL for males at screening
Neutrophil count ≥1.5 × 10\^9/L at screening
Creatinine clearance rate ≥40 mL/min at screening (according to the Cockcroft-Gault formula)
Males and females of childbearing potential, as well as all women <2 years after the onset of menopause, must agree to use an acceptable form of birth control until 60 days following the last dose of the study drug, and females must agree to not breastfeed during the study
Written informed consent obtained from the subject and ability for the subject to comply with the requirements of the study

You may not qualify if…

Any contraindications to interferon alfa or hypersensitivity to interferon alfa
Subjects who stopped prior to interferon alfa therapy due to low efficacy or poor tolerability
Subjects with severe or serious diseases that the Investigator determines may affect the subject's participation in this study
History of major organ transplantation
Pregnant or breastfeeding women
Subjects with any other diseases that the Investigator determines will affect the study results or may weaken the compliance to protocol, including but not limited to:
Prior or current autoimmune thyroid disease (clinical symptoms of hyper- or hypo-thyroidism), except subjects with controlled thyroid replacement therapy, could be enrolled
Other documented autoimmune diseases (such as hepatitis, immune thrombocytopenia [ITP], scleroderma, psoriasis, or any autoimmune arthritis)
Clinically significant pulmonary infiltration, infectious pneumonia, and non-infectious pneumonia, or a past history of interstitial pneumonia at screening
Active infection with systemic manifestations (e.g., presence of bacteria, fungi, and/or human immunodeficiency virus [HIV] at screening, excluding hepatitis B [HBV] and/or hepatitis C [HCV] at screening)
Evidence of severe retinopathy (e.g., cytomegalovirus [CMV]-induced retinitis, macular degeneration) or clinically significant eye diseases (due to diabetes or hypertension)
History or presence of clinically relevant depression per Investigator's judgment
Previously had suicidal attempts or has any risk for suicidal tendency at screening
Poorly controlled diabetes defined as HbA1c >8.0% for at least 1 year
Active thromboembolic complications caused by PV and abdominal hemorrhage in the active phase
History of any malignancy within 5 years (except adequately treated non-melanoma skin cancer, prostate cancer status post resection with an undetectable prostate-specific antigen (PSA), curative treated in-situ cancer of the cervix, ductal carcinoma in situ (DCIS) of the breast, Stage 1 Grade 1 endometrial carcinoma, or other solid tumors including lymphomas (without bone marrow involvement) curatively treated with no evidence of disease for ≥2 years prior to study)
History of alcohol or drug abuse in the past year
History or evidence of post-polycythemia vera-myelofibrosis (PPV-MF), essential thrombocythemia, or any non-PV MPN
Presence of blast cells in the peripheral blood in the past 12 weeks
Use any investigational drug <4 weeks prior to the first dose of study drug, or not recovered from effects of prior administration of any investigational drug
Any subject requiring a legally authorized representative

Where it is running

Baptist MD Anderson — Jacksonville, Florida, United States
Fort Wayne Medical Oncology and Hematology — Fort Wayne, Indiana, United States
University of Kansas Medical Center — Westwood, Kansas, United States
Mercy Health — Paducah, Kentucky, United States
Tulane University Medical Center — New Orleans, Louisiana, United States
American Oncology Partners of Maryland PA (Center for Cancer & Blood Disorders) — Bethesda, Maryland, United States
Washington University School of Medicine — St Louis, Missouri, United States
Astera HealthCare — East Brunswick, New Jersey, United States
Mount Sinai — New York, New York, United States
Montefiore Medical Center — The Bronx, New York, United States
University of North Carolina Lineberger Comprehensive Cancer Center — Chapel Hill, North Carolina, United States
East Carolina University — Greenville, North Carolina, United States
Wake Forest Baptist Medical Center — High Point, North Carolina, United States
University of Tennessee Health Science Center — Memphis, Tennessee, United States
MD Anderson — Houston, Texas, United States
University of Utah — Salt Lake City, Utah, United States
University of Virginia - Emily Couric Cancer Center — Charlottesville, Virginia, United States
Tom Baker Cancer Centre — Calgary, Alberta, Canada
St. Paul's Hospital — Vancouver, British Columbia, Canada
Juravinski Cancer Center - Hamilton Health Sciences — Hamilton, Ontario, Canada
The Ottawa Hospital — Ottawa, Ontario, Canada
St. Michael's Hospital — Toronto, Ontario, Canada
Princess Margaret Hospital — Toronto, Ontario, Canada

Full record on ClinicalTrials.gov

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