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Cyklokapron (TRANEXAMIC ACID)

Exela Pharma · FDA-approved approved Small molecule Under review Quality 10/100

Cyklokapron (generic name: TRANEXAMIC ACID) is a Antifibrinolytic Agent [EPC] Small molecule drug developed by Exela Pharma. It is currently FDA-approved (first approved 1986) for Contraception, Endometriosis, Female hypogonadism syndrome.

Tranexamic acid works by binding to plasminogen and preventing its conversion to plasmin, thereby inhibiting fibrinolysis.

Cyklokapron, also known as tranexamic acid, is a small molecule that inhibits plasminogen, a protein involved in blood clot breakdown. It is used to treat or prevent conditions such as blood loss, postoperative complications, and osteoarthritis knee pain.

At a glance

Generic nameTRANEXAMIC ACID
SponsorExela Pharma
Drug classAntifibrinolytic Agent [EPC]
TargetPlasminogen
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1986

Mechanism of action

Tranexamic acid is synthetic lysine amino acid derivative, which diminishes the dissolution of hemostatic fibrin by plasmin. In the presence of tranexamic acid, the lysine receptor binding sites of plasmin for fibrin are occupied, preventing binding to fibrin monomers, thus preserving and stabilizing fibrins matrix structure.The antifibrinolytic effects of tranexamic acid are mediated by reversible interactions at multiple binding sites within plasminogen. Native human plasminogen contains to lysine binding sites with low affinity for tranexamic acid (Kd 750 umol/L) and with high affinity (Kd 1.1 umol/L). The high affinity lysine site of plasminogen is involved in its binding to fibrin. Saturation of the high affinity binding site with tranexamic acid displaces plasminogen from the surface of fibrin. Although plasmin may be formed by conformational changes in plasminogen, binding to and dissolution of the fibrin matrix is inhibited.

Approved indications

Common side effects

Drug interactions

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Cyklokapron

What is Cyklokapron?

Cyklokapron (TRANEXAMIC ACID) is a Antifibrinolytic Agent [EPC] drug developed by Exela Pharma, indicated for Contraception, Endometriosis, Female hypogonadism syndrome.

How does Cyklokapron work?

Tranexamic acid works by binding to plasminogen and preventing its conversion to plasmin, thereby inhibiting fibrinolysis.

What is Cyklokapron used for?

Cyklokapron is indicated for Contraception, Endometriosis, Female hypogonadism syndrome, Hemorrhaging in Hemophilia, Menorrhagia.

Who makes Cyklokapron?

Cyklokapron is developed and marketed by Exela Pharma (see full Exela Pharma pipeline at /company/exela-pharma).

What is the generic name of Cyklokapron?

TRANEXAMIC ACID is the generic (nonproprietary) name of Cyklokapron.

What drug class is Cyklokapron in?

Cyklokapron belongs to the Antifibrinolytic Agent [EPC] class. See all Antifibrinolytic Agent [EPC] drugs at /class/antifibrinolytic-agent-epc.

When was Cyklokapron approved?

Cyklokapron was first approved on 1986.

What development phase is Cyklokapron in?

Cyklokapron is FDA-approved (marketed).

What are the side effects of Cyklokapron?

Common side effects of Cyklokapron include Thromboembolic events, Convulsion, Chromatopsia, Visual impairment, Anaphylaxis or anaphylactoid reaction, Hypotension.

What does Cyklokapron target?

Cyklokapron targets Plasminogen and is a Antifibrinolytic Agent [EPC].

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing