MedPath

Conestat alfa

Generic Name
Conestat alfa
Brand Names
Ruconest
Drug Type
Biotech
CAS Number
80295-38-1
Unique Ingredient Identifier
5QS67N4551

Overview

C1 Esterase Inhibitor (Recombinant) is a recombinant analogue of endogenous complement component-1 esterase inhibitor (rhC1INH), purified from the milk of transgenic rabbits. The primary function of endogenous C1INH is to regulate the activation of the complement and contact system pathways. It does this through inhibition of several target proteases within these pathways including activated C1s, kallikrein, factor XIIa and factor XIa. C1 esterase inhibitor has also been shown to inhibit the action of thrombin within the coagulation pathway, and tPA and plasmin within the fibrinolytic pathway. Deficiency of C1-inhibitor allows for increased plasma kallikrein activation and subsequent production of bradykinin. Additionally, C4 and C2 cleavage occurs resulting in auto-activation of the complement system. Down-stream effects of the lack of enzyme inhibition by C1 esterase inhibitor results in swelling due to leakage of fluid from blood vessels into connective tissue and consequently the presentation of hereditary angioedema (HAE). Marketed as the product Ruconest (FDA), this drug is indicated for the treatment of acute attacks of hereditary angioedema (HAE) due to C1 esterase inhibitor deficiency in adults. Intravenous replacement of C1 esterase inhibitor results in reversal of acute symptoms of HAE.

Indication

For the treatment of acute attacks of hereditary angioedema (HAE) due to C1 esterase inhibitor deficiency in adults.

Associated Conditions

  • Acute attacks of hereditary angioedema

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/11/15
Phase 4
Completed
Bernstein Clinical Research Center
2024/11/07
Phase 3
Not yet recruiting
2021/01/12
Phase 4
UNKNOWN
2020/08/28
Phase 2
Completed
2020/06/04
Phase 2
Terminated
University Hospital, Basel, Switzerland
2019/01/02
Phase 1
UNKNOWN
2018/10/05
N/A
Completed
2016/08/16
Phase 2
Completed
University Hospital, Basel, Switzerland
2011/05/25
Phase 2
Completed
2010/08/25
Phase 3
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Pharming Healthcare Inc.
71274-350
INTRAVENOUS
2100 U in 1 1
4/30/2020
Tjoapack Netherlands BV
69913-350
INTRAVENOUS
2100 U in 1 1
10/24/2022

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
Authorised
10/28/2010

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
RUCONEST 2100 U POLVO PARA SOLUCION INYECTABLE
110641001
POLVO PARA SOLUCIÓN INYECTABLE
Uso Hospitalario
Not Commercialized
RUCONEST 2100 U POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE
110641002
POLVO Y DISOLVENTE PARA SOLUCIÓN INYECTABLE
Uso Hospitalario
Not Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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