Language of document : ECLI:EU:T:2013:221





Order of the President of the General Court of 25 April 2013 — AbbVie v EMA

(Case T‑44/13 R)

Application for interim measures — Access to documents — Regulation (EC) No 1049/2001 — Documents held by the EMA containing information submitted by an undertaking as part of its application for authorisation to place a medicinal product on the market — Decision to grant a third party access to the documents — Application for suspension of operation of a measure — Urgency — Prima facie case — Weighing up of interests

1.                     Application for interim measures — Suspension of operation of a measure — Interim measures — Conditions for granting — Prima facie case — Urgency — Serious and irreparable damage — Cumulative nature — Weighing-up of the interests — Discretion of the court hearing the application for interim relief (Arts 256(1) TFEU, 278 TFEU and 279 TFEU; Rules of Procedure of the General Court, Art. 104(2)) (see paras 34-36)

2.                     Application for interim measures — Suspension of operation of a measure — Conditions for granting — Balancing of all the interests involved — Suspension of operation of a decision of the European Medicines Agency granting a third party access to reports of clinical trials — Need to maintain the effectiveness of the decision of the General Court in the action in the main proceedings (Art. 278 TFEU) (see paras 39-44)

3.                     Application for interim measures — Suspension of operation of a measure — Interim measures — Conditions for granting — Urgency — Serious and irreparable damage — Risk of serious and irreparable damage to fundamental rights (Arts 6(1), first para., TEU, 278 TFEU, 279 TFEU and 339 TFEU; Charter of Fundamental Rights of the European Union, Arts 7 and 47) (see paras 47-48, 52)

4.                     Application for interim measures — Suspension of operation of a measure — Conditions for granting — Prima facie case — Examination prima facie of the pleas in law put forward in support of the main action — Action against a decision of the European Medicines Agency granting a third party access to reports of clinical trials — Pleas concerning the confidentiality of information covered by business secrecy — Pleas revealing the existence of complex legal questions — Pleas not prima face unfounded (Arts 278 TFEU and 339 TFEU; Charter of Fundamental Rights of the European Union, Art. 7) (see paras 54, 55, 65-70)

Re:

APPLICATION, in essence, for suspension of operation of EMA Decision EMA/748792/2012 of 14 January 2013, granting a third party access to certain documents containing information submitted as part of an application for authorisation to place the medicinal product Humira, used to treat Crohn’s Disease, on the market, pursuant to Regulation (EC) No 1049/2001 of the European Parliament and of the Council of 30 May 2001 regarding public access to European Parliament, Council and Commission documents (OJ 2001 L 145, p. 43).

Operative part

1.

The operation of EMA Decision EMA/748792/2012 of 14 January 2013 of the European Medicines Agency (EMA), granting a third party access to Clinical Study Reports M02-404, M04-691 and M05-769, submitted as part of an application for authorisation to place the medicinal product Humira, used to treat Crohn’s Disease, on the market, pursuant to Regulation (EC) No 1049/2001 of the European Parliament and of the Council of 30 May 2001 regarding public access to European Parliament, Council and Commission documents, is suspended.

2.

The EMA is ordered not to disclose the documents referred to in point 1 of the operative part of this order.

3.

Costs are reserved.