Rapamune

Active Substance: sirolimus
Common Name: sirolimus
ATC Code: L04AA10
Marketing Authorisation Holder: Pfizer Limited
Active Substance: sirolimus
Status: Authorised
Authorisation Date: 2001-03-13
Therapeutic Area: Kidney Transplantation Graft Rejection
Pharmacotherapeutic Group: Immunosuppressants

Therapeutic Indication

Rapamune is indicated for the prophylaxis of organ rejection in adult patients at low to moderate immunological risk receiving a renal transplant.

It is recommended that Rapamune be used initially in combination with ciclosporin microemulsion and corticosteroids for two to three months.

Rapamune may be continued as maintenance therapy with corticosteroids only if ciclosporin microemulsion can be progressively discontinued.

What is Rapamune?

Rapamune is a medicine that contains the active substance sirolimus. It is available as an oral solution (1 mg/ml) and triangular tablets (tan: 0.5 mg; white: 1 mg; yellow: 2 mg).

What is Rapamune used for?

Rapamune is used to prevent the body from rejecting a newly transplanted kidney. It is used in adults (aged 18 years or over) who are at a low to moderate risk of rejection. It is recommended that Rapamune be used with ciclosporin and corticosteroids (other medicines to prevent organ rejection) for two to three months. After this period, Rapamune can be used as maintenance treatment together with corticosteroids, but only if ciclosporin treatment can be stopped.

The medicine can only be obtained with a prescription.

How is Rapamune used?

Rapamune treatment should be started by and remain under the guidance of a doctor who is a qualified specialist in transplantation.

Rapamune is given as an initial dose of 6 mg as soon as possible after the transplant, followed by 2 mg once a day for two to three months. The levels of sirolimus in the patient’s blood should be monitored, and the dose of Rapamune should be adjusted to obtain the appropriate levels of sirolimus (4 to 12 ng/ml). Rapamune should be taken four hours after each ciclosporin dose. Patients should always take Rapamune consistently, either with or without food.

After this period, Rapamune can be used as ‘maintenance therapy’ in patients who are able to stop ciclosporin. In these cases, the dose of ciclosporin should be gradually reduced to zero over four to eight weeks, and the dose of Rapamune increased to obtain blood levels of sirolimus of about 12 to 20 ng/ml. On average, the dose of Rapamune needs to be increased fourfold.

How does Rapamune work?

The active substance in Rapamune, sirolimus, is an immunosuppressive agent (a medicine that reduces the activity of the immune system). It works by blocking a protein called ‘mammalian target of rapamycin’ (mTOR). In the body, sirolimus attaches to a protein that is found inside cells to make a ‘complex’. This complex then blocks mTOR. Since mTOR is involved in the multiplication of activated T-lymphocytes (white blood cells that are responsible for attacking the transplanted organ), Rapamune reduces the number of these cells, reducing the risk of organ rejection.

How has Rapamune been studied?

Rapamune has been studied in two main studies involving a total of 1,295 patients who were having a kidney transplant and were at low to moderate risk of rejection. The first study compared Rapamune oral solution with azathioprine (another anti-rejection medicine) in 719 patients, and the second compared it with placebo (a dummy treatment) in 576 patients. The medicines were used as an add-on to ciclosporin and corticosteroids. The effectiveness was measured by looking at the number of treatment failures (rejection or loss of the new kidney, or death) after six months.

Two studies looked at Rapamune as maintenance treatment for up to five years in a total of 765 patients who had responded to an initial two- to three-month course of treatment and who were able to stop their dose of ciclosporin.

One additional study compared the ability of the oral solution and the tablets to prevent rejection.

What benefit has Rapamune shown during the studies?

Rapamune was more effective than placebo or azathioprine, when they were added to ciclosporin and corticosteroids. In the first study, 19% of the patients adding Rapamune had failed treatment after six months (53 out of 284), compared with 32% of those adding azathioprine (52 out of 161). In the second study, 30% of the patients adding Rapamune failed treatment (68 out of 277), compared with 48% of those adding placebo (62 out of 130).

The maintenance studies showed that long-term treatment with Rapamune was effective in helping the new kidney to survive, with an improvement in how well the new kidney worked and an improvement in blood pressure when ciclosporin treatment was stopped.

The additional study showed that the oral solution and the tablets were equally effective in preventing rejection.

What is the risk associated with Rapamune?

The most common side effects with Rapamune (seen in more than 1 patient in 10) are urinary-tract infection (infection of the structures that carry urine), thrombocytopenia (low blood platelet counts), anaemia (low red-blood-cell counts), hypokalaemia (low blood potassium levels), hypophosphataemia (low blood phosphate levels), hypercholesterolaemia (high blood cholesterol levels), hyperglycaemia (high blood sugar levels), hypertriglyceridaemia (high blood levels of triglycerides, a type of fat), headache, lymphocele (fluid collection around the kidney), hypertension (high blood pressure), abdominal pain (stomach ache), diarrhoea, constipation, nausea (feeling sick), acne, arthralgia (joint pain), peripheral oedema (swelling, especially of the ankles and feet), pyrexia (fever), pain, increased blood lactate dehydrogenase levels (a marker of tissue breakdown) and increased blood creatinine levels (a marker of kidney problems). Because it reduces the activity of the immune system, Rapamune can also increase the risk of developing cancer, especially lymphoma and skin cancer. For the full list of all side effects reported with Rapamune, see the package leaflet.

Rapamune should not be used in people who may be hypersensitive (allergic) to sirolimus or any of the other ingredients. Patients allergic to peanut or soya must not take Rapamune oral solution because the solution contains soya oil.

Why has Rapamune been approved?

The CHMP decided that Rapamune’s benefits are greater than its risks and recommended that it be given marketing authorisation.

Other information about Rapamune

The European Commission granted a marketing authorisation valid throughout the European Union for Rapamune on 14 March 2001.

For more information about treatment with Rapamune, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.

Source: European Medicines Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide
(web4)