Basic Information
EMA regulatory identification and product classification information
EMA Identifiers
Overview Summary
Comprehensive product overview and regulatory summary
Vocabria is used together with another medicine called rilpivirine to treat adults and adolescents aged 12 years and older infected with human immunodeficiency virus type 1 (HIV-1), a virus that causes acquired immune deficiency syndrome (AIDS). It is used when the infection is under control with antiretroviral medicines (medicines for HIV). Adolescents must weigh at least 35 kg to take Vocabria.
Vocabria contains the active substance cabotegravir.
Active Substances (4)
Cabotegavir sodium
Cabotegravir
cabotegavir sodium
cabotegravir
Documents (14)
Vocabria : EPAR - Medicine overview
January 5, 2021
OVERVIEW_DOCUMENT
Vocabria : EPAR - Public assessment report
January 5, 2021
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
CHMP summary of positive opinion for Vocabria
October 16, 2020
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Vocabria : EPAR - Risk management plan
January 5, 2021
RISK_MANAGEMENT_PLAN_SUMMARY
Vocabria : EPAR - All authorised presentations
January 5, 2021
AUTHORISED_PRESENTATIONS
Vocabria-H-C-PSUSA-00010900-202203 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
January 12, 2023
CHANGES_SINCE_INITIAL_AUTHORISATION
Vocabria-H-C-004976-II-0022 : EPAR - Assessment report - Variation
January 22, 2025
CHANGES_SINCE_INITIAL_AUTHORISATION
Vocabria : EPAR - Public assessment report
January 5, 2021
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP post-authorisation summary of positive opinion for Vocabria (II-22)
December 13, 2024
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP summary of positive opinion for Vocabria
October 16, 2020
CHANGES_SINCE_INITIAL_AUTHORISATION
Vocabria-H-C-PSUSA-00010900-202109 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
January 27, 2022
CHANGES_SINCE_INITIAL_AUTHORISATION
Vocabria-H-C-PSUSA-00010900-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation
December 19, 2024
CHANGES_SINCE_INITIAL_AUTHORISATION
Vocabria : EPAR - Product Information
January 5, 2021
DRUG_PRODUCT_INFORMATION
Vocabria : EPAR - Procedural steps taken and scientific information after authorisation
March 11, 2021
CHANGES_SINCE_INITIAL_AUTHORISATION
Overview Q&A (7)
Question
How does Vocabria work?
Answer
Vocabria is an integrase inhibitor. This is a medicine that blocks an enzyme called integrase that the virus needs to make new copies of itself in the body. By blocking this enzyme, Vocabria, taken together with rilpivirine, reduces the amount of HIV in the blood and keeps it at a low level. Vocabria does not cure HIV infection or AIDS, but it can hold off damage to the immune system and the development of infections and diseases associated with AIDS.
Question
What measures are being taken to ensure the safe and effective use of Vocabria?
Answer
The company that markets Vocabria will carry out 2 studies on how the medicine is used and its effectiveness. The outcomes for patients who switch to other treatments after taking Vocabria will also be studied.
Recommendations and precautions to be followed by healthcare professionals and patients for the safe and effective use of Vocabria have also been included in the summary of product characteristics and the package leaflet.
As for all medicines, data on the use of Vocabria are continuously monitored. Side effects reported with Vocabria are carefully evaluated and any necessary action taken to protect patients.
Question
Other information about Vocabria
Answer
Vocabria received a marketing authorisation valid throughout the EU on 17 December 2020.
Question
How is Vocabria used?
Answer
Vocabria is available as tablets to be taken by mouth or as an injection given into a muscle of the hip or buttock. After being injected, the active substance is released slowly over a few weeks into the bloodstream.
Before starting treatment, the doctor ensures that the patient agrees to keep to the schedule of injections because this is important to keep the virus under control and there is a risk that levels of the virus could increase or the virus could become resistant to treatment if doses are missed.
Cabotegravir and rilpivirine tablets are taken daily by mouth for one month, after which Vocabria and rilpivirine injections are given monthly or every 2 months.
If treatment with Vocabria is stopped, another treatment to suppress the virus must be started to minimise the risk that the virus could become resistant to treatment.
Vocabria can only be obtained with a prescription and should be prescribed by a doctor who has experience in the management of HIV infection.
For more information about using Vocabria, including the schedule for the injections, see the package leaflet or contact your doctor or pharmacist.
Question
What benefits of Vocabria have been shown in studies?
Answer
Vocabria, taken together with rilpivirine, was as effective as other HIV medicines in maintaining HIV-1 level in the blood (viral load) below a defined level (less than 50 HIV-1 RNA copies/ml) in 3 main studies involving adults with HIV-1 infection. The studies involved patients who had not taken HIV medicines before or who had been taking these medicines for at least 6 months.
In the first two studies, patients were treated with Vocabria and rilpivirine or with combinations of other medicines. After 48 weeks of treatment, the HIV-1 level was above the limit in 1.9% of patients (11 out of 591) taking monthly injections of Vocabria and rilpivirine and in 1.7% of patients (10 out of 591) taking other medicines.
The third study showed that injections of Vocabria and rilpivirine given monthly or every 2 months were similarly effective. After 48 weeks of treatment, the HIV-1 level was above the limit in 1.7% of patients (9 out of 522) given injections every 2 months, compared with 1% of patients (5 out of 523) who had monthly injections.
A further study showed that giving Vocabria to adolescents aged 12 years and older and weighing at least 35 kg resulted in blood levels of the active substance similar to those seen in adults. Therefore, the medicine is expected to have similar effects in adolescents.
Question
What are the risks associated with Vocabria?
Answer
For the full list of side effects and restrictions with Vocabria, see the package leaflet.
The most common side effects with Vocabria and rilpivirine monthly injections (which may affect more than 1 in 10 people) include injection site reactions, headache and fever.
Vocabria must not be used with the following medicines as they may lead to reduced blood levels of the medicine, reducing its effectiveness:
- carbamazepine, oxcarbazepine, phenobarbital and phenytoin (medicines for epilepsy);
- rifampicin and rifapentine (antibiotics).
Question
Why is Vocabria authorised in the EU?
Answer
Injections of Vocabria every month or every 2 months may be more convenient for patients than taking medicines every day. Studies showed that the medicine was as effective at keeping the virus level low as other standard medicines. It is important that patients keep to the schedule of injections to avoid the virus becoming resistant to treatment, and further studies will determine whether this is happening while the medicine is on the market.