This trial is active, not recruiting.

Condition paroxysmal nocturnal hemoglobinuria (pnh)
Treatments study drug - alxn1210
Phase phase 1/phase 2
Sponsor Alexion Pharmaceuticals
Start date November 2015
End date July 2016
Trial size 13 participants
Trial identifier NCT02598583, ALXN1210-PNH-103


The primary purpose of this study is to evaluate the safety, tolerability and efficacy of multiple IV doses of ALXN1210 administered to patients with PNH

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Intervention model single group assignment
Masking open label
Primary purpose treatment
Study Drug - ALXN1210
study drug - alxn1210
Cohort 1: Intrapatient dose escalation to therapeutic dose level
Study Drug - ALXN1210
study drug - alxn1210
Cohort 2: Intrapatient dose escalation to therapeutic dose level

Primary Outcomes

To evaluate the safety as measured by the number of treatment-emergent and related adverse events as assessed by CTCAE (v4.03).
time frame: 24 weeks
Efficacy as measured by the percentage change in lactate dehydrogenase or LDH levels from baseline to Day 169 during treatment with ALXN1210.
time frame: 24 weeks

Secondary Outcomes

Time to maximal concentration of ALXN1210 in blood (tmax)
time frame: 24 weeks
Area Under the plasma concentration versus time Curve (AUC) of ALXN1210.
time frame: 24 weeks
Peak Plasma Concentration (Cmax) of ALXN1210.
time frame: 24 weeks
ALXN1210 elimination half-life (t1/2) in blood.
time frame: 24 weeks
Change from baseline in concentration of complement factor 5 (C5). Change from baseline in serum levels of terminal complement activity
time frame: 24 weeks
Development of antibodies against ALXN1210.
time frame: Up to 128 weeks

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: 1. Male or female ≥ 18 years of age 2. PNH diagnosis confirmed by documented high-sensitivity flow cytometry 3. Documented meningococcal vaccination not more than 3 years prior to dosing 4. Female patients of childbearing potential must use highly effective contraception starting at screening and continuing until at least 6 months after the last dose of ALXN1210. 5. Willing and able to give written informed consent and comply with the study visit schedule Exclusion Criteria: 1. Treatment with a complement inhibitor at any time 2. Females who are pregnant, breastfeeding or who have a positive pregnancy test at screening or Day 1 3. Participation in a clinical study within 30 days before initiation of dosing on Day 1, or use of any experimental therapy within 30 days prior to dosing on Day, or within 5 half lives of the product, whichever is greater 4. History of allergy to excipients of ALXN1210 or known allergy to Chinese hamster ovary (CHO) cell proteins 5. Inability to comply with study requirements 6. History of any clinically significant cardiac, hepatic, immunologic, pulmonary, or rheumatoid disease that, in the Investigator's judgment, would preclude participation 7. Other unspecified reasons that, in the opinion of the Investigator or Sponsor, make the patient unsuitable for enrollment

Additional Information

Official title An Open-Label, Intrapatient, Dose-Escalation Study to Evaluate the Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of ALXN1210 Administered Intravenously to Patients With Paroxysmal Nocturnal Hemoglobinuria
Trial information was received from ClinicalTrials.gov and was last updated in October 2016.
Information provided to ClinicalTrials.gov by Alexion Pharmaceuticals.