Coversin in PNH in Patients With Resistance to Eculizumab Due to Complement C5 Polymorphisms

Phase 2

Completed

• Conditions: Paroxysmal Nocturnal Hemoglobinuria (PNH)
• Interventions: Drug: Coversin

• Registration Number: NCT03427060
• Lead Sponsor: AKARI Therapeutics

Brief Summary

Coversin in Paroxysmal Nocturnal Hemoglobinuria (PNH) in patients with resistance to Eculizumab due to complement C5 polymorphisms.

Detailed Description

Coversin, a small protein complement C5 inhibitor which prevents the cleavage of C5 by C5 convertase into C5a and C5b, will be used in an open label, non-comparative clinical trial in patients with PNH and proven resistance to eculizumab due to C5 polymorphisms. Patients will be treated with Coversin by daily subcutaneous injection for 6 months in order to determine the safety and efficacy of the drug in these circumstances. If satisfactory control of the PNH is achieved, and at the discretion of the Principal Investigator (PI), patients will have the option of remaining on Coversin and being entered into the long term follow-up study.

Study Timeline

• Study First Submitted: 2018-01-24
• Study First Submitted QC: 2018-02-02
• Study First Posted: 2018-02-09
• Study Start: 2018-05-14
• Primary Completion: 2018-11-15
• Study Completion: 2021-02-03
• Status Verified: 2024-12
• Results First Submitted: 2025-03-10
• Results First Submitted QC: 2025-04-17
• Last Update Submitted: 2025-04-17
• Results First Posted: 2025-05-04
• Last Update Posted: 2025-05-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1

Inclusion Criteria

1. Patients with known PNH.
2. Aged 18 and above. No upper age limit.
3. Lactate dehydrogenase (LDH) ≥1.5 upper limit of normal.
4. Must agree to use two methods of contraception that are ≥99% effective in preventing pregnancy.
5. Resistance to eculizumab (Soliris®).
6. Voluntary written informed consent.
7. Willing to self-inject Coversin daily.
8. Willing to receive appropriate prophylaxis against Neisseria infection.
9. Willing to avoid prohibited medications for duration of study.

Exclusion Criteria

1. Subjects with body weight <50 kg (110 lb) or >100 kg (220 lb).
2. Pregnancy or breast feeding (females).
3. Known allergy to ticks or severe reaction to arthropod venom (e.g. bee or wasp venom).
4. Unresolved Neisseria meningitidis infection.
5. Patients who have not received adequate immunization against Neisseria meningitides.
6. Impaired hepatic function.
7. Patients with impaired renal function.
8. Failure to satisfy the Principal Investigator (PI) of fitness to participate for any other reason.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Coversin treatment	Coversin	Coversin - 22.5mg followed by 45mg for 6 months.

Primary Outcome Measures

Name	Time	Method
Measurement of Serum Lactate Dehydrogenase (LDH)	Baseline to Day 186	Measurement of serum lactate dehydrogenase (LDH)

Secondary Outcome Measures

Name	Time	Method
Percentage Change in Haemoglobin (Hb) Compared to Screening	Baseline to Day 186	Percentage change in the haemoglobin (Hb) value at each study visit compared to screening
Number of Packed Red Blood Cells (PRBC) Transfusions	Baseline to Day 180	Number of units of packed red blood cells (PRBC) transfusions

Trial Locations

Locations (1)

Memorial Sloan Kettering Cancer Center; 🇺🇸 New York, New York, United States