Pemetrexed Krka

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On 22 March 2018, the Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion, recommending the granting of a marketing authorisation for the medicinal product Pemetrexed Krka, intended for the treatment of malignant pleural mesothelioma and non-small cell lung cancer. The applicant for this medicinal product is Krka d.d.

Pemetrexed Krka will be available as a powder (100 mg and 500 mg) for concentrate for solution for infusion. The active substance of Pemetrexed Krka, pemetrexed, is a multi-targeted anti-cancer antifolate agent (ATC code: L01BA04) that exerts its action by disrupting crucial folate-dependent metabolic processes essential for cell replication.

Pemetrexed Krka is a generic of Alimta, which has been authorised in the EU since 20 September 2004. Studies have demonstrated the satisfactory quality of Pemetrexed Krka. Since Pemetrexed Krka is administered intravenously and is 100% bioavailable, a bioequivalence study versus the reference product Alimta was not required. 

The full indication is:

"Malignant pleural mesothelioma

Pemetrexed Krka in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma.

Non-small cell lung cancer

Pemetrexed Krka in combination with cisplatin is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology (see section 5.1).

Pemetrexed Krka is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy (see section 5.1).

Pemetrexed Krka is indicated as monotherapy for the second-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology (see section 5.1)."

It is proposed that Pemetrexed Krka be subject to prescription and administered under the supervision of physicians experienced in the use of anti-cancer chemotherapy.

Detailed recommendations for the use of this product will be described in the summary of product characteristics (SmPC), which will be published in the European public assessment report (EPAR) and made available in all official European Union languages after the marketing authorisation has been granted by the European Commission.

Name Language First published Last updated
CHMP summary of positive opinion for Pemetrexed Krka (English only) 2018-03-23  

Key facts

Product details for Pemetrexed Krka
NamePemetrexed Krka
INN or common name

pemetrexed

Therapeutic area Carcinoma, Non-Small-Cell LungMesothelioma
Active substance

pemetrexed disodium

Date opinion adopted22/03/2018
Company name

Krka d.d.

StatusPositive
Application typeInitial authorisation