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      German Agency for HTA at the German Institute for Medical Documentation and Information
      Gesundheit Osterreich GmbH
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      State Health Care Accreditation Agency under the Ministry of Health of the Republic of Lithuania
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      Swiss Federal Office of Public Health (FOPH)
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Welcome to the international HTA database

CSV RIS
Showing [23529 Records] Selected Records [0 Hits] [Clear]
Year Source Title
2019     Institute for Clinical Effectiveness and Health Policy (IECS) [Pirfenidone in pulmonary fibrosis]
2011     Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG) [Pirfenidone - Benefit assessment according to §35a Social Code Book V (dossier assessment)]
2011     Institute for Clinical Effectiveness and Health Policy (IECS) [Pipeline embolization device]
2014     Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG) [Pilot study: conjoint analysis in the indication "hepatitis C"]
2013     Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG) [Pilot study: analytic hierarchy process in the indication "major depression"]
2014     Basque Office for Health Technology Assessment (OSTEBA) [Pilot study to identify and assess obsolete health technologies from emerging technologies identification databases]
2015     National Evidence-based Healthcare Collaborating Agency (NECA) [Pilot study for understanding the present situation of decorative tattoos]
2009     Committee for New Health Technology Assessment (CNHTA) [PIGA (Phosphatidyl inositol glycan-Class A) mutation analysis]
2012     Haute Autorite de sante (HAS) [Physiotherapeutic treatment of lymphoedema and shoulder stiffness after breast cancer treatment]
2020     Canary Health Service [Physical exercise intervention in older hospitalized patients for the prevention of functional and cognitive deterioration during hospital admission]
2009     Agencia de Evaluacion de Tecnologias Sanitarias (AETS) [Physical disease in schizophrenia: systematic review and analysis of hospital records]
2018     Swedish Agency for Health Technology Assessment and Assessment of Social Services (SBU) [Phototherapy and systemic treatment for moderate to severe psoriasis]
2008     Scientific Advice Unit, avalia-t; The Galician Health Knowledge Agency (ACIS) [Photoselective vaporization for benign prostatic hyperplasia with KTP (potassium-titanyl-phosphate) laser or GreenLight]
2014     Scientific Advice Unit, avalia-t; The Galician Health Knowledge Agency (ACIS) [Photopheresis in treatment of steroid-refractory acute graft-versus-host disease]
2002     Danish Centre for Evaluation and Health Technology Assessment (DACEHTA) [Photodynamic treatment of subretinal new vessels of choroidal origin in age-related macular degeneration - an HTA]
2020     National Committee for Technology Incorporation (CONITEC) [Photodynamic therapy for non-melanoma skin cancer]
2012     Institute for Clinical Effectiveness and Health Policy (IECS) [Photodynamic therapy for non-melanocytic skin cancer treatment]
2005     Secretaria de Ciencia, Tecnologia e Insumos Estrategicos, Departamento de Ciencia e Tecnologia (DECIT-CGATS ) [Photodynamic therapy for neovascular age-related macular degeneration]
2012     Institute for Clinical Effectiveness and Health Policy (IECS) [Photodynamic therapy for lung cancer]
2012     Institute for Clinical Effectiveness and Health Policy (IECS) [Photodynamic therapy for head and neck cancer treatment]
2012     Institute for Clinical Effectiveness and Health Policy (IECS) [Photodynamic therapy for colon cancer]
2011     Committee for New Health Technology Assessment (CNHTA) [Photodynamic therapy for bladder, cervix and lung cancer]
2012     Institute for Clinical Effectiveness and Health Policy (IECS) [Photodynamic therapy for barrett's esophagus and esophageal cancer]
2009     Unidad de Evaluacion de Tecnologias Sanitarias (UETS) [Photodynamic therapy effectiveness, safety and cost-effectiveness in oesophagus cancer and Barrett oesophagus treatment]
2009     Unidad de Evaluacion de Tecnologias Sanitarias (UETS) [Photodynamic therapy effectiveness and safety in nonmelanoma skin cancer]
2018     Institute for Clinical Effectiveness and Health Policy (IECS) [Phlebotonics for venous insufficiency]
2009     Committee for New Health Technology Assessment (CNHTA) [PHEX gene, Mutation[Sequencing]]
2011     Scientific Advice Unit, avalia-t; The Galician Health Knowledge Agency (ACIS) [Pharyngeal pH monitoring by Dx-pH measurement system]
2022     Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG) [Pharmacotherapeutic interventions - Evidence report on the S3 guideline "Cannabis-related disorders"]
2011     Catalan Agency for Health Information, Assessment and Quality (CAHIAQ -formerly CAHTA) [Pharmacologically-induced voluntary interruption of pregnancy]
2002     Basque Office for Health Technology Assessment (OSTEBA) [Pharmacological treatment of migraines. Qualitative study]
2020     Swedish Agency for Health Technology Assessment and Assessment of Social Services (SBU) [Pharmacological treatment of common pain conditions in older persons]
2012     Catalan Agency for Health Information, Assessment and Quality (CAHIAQ -formerly CAHTA) [Pharmacological treatment for controlled ovarian hyperstimulation in vitro fertilization]
2018     Swedish Agency for Health Technology Assessment and Assessment of Social Services (SBU) [Pharmacological interventions in forensic psychiatry]
2010     Gesundheit Osterreich GmbH (GOeG) [Pharmacological interactions between acetylcholinesterase inhibitors for treatment of dementia and further drugs occurring in patients of advanced age]
2008     German Agency for Health Technology Assessment at the German Institute for Medical Documentation and Information (DAHTA DIMDI) [Pharmacogenomics bias - systematic distortion of study results by genetic heterogeneity]
2013     The Netherlands Organisation for Health Research and Development (ZonMw) [Pharmacogenetic testing in the clinical setting: is screening for TPMT genotype a cost-effective treatment strategy? The first prospective randomized controlled trial within the Dutch health care system]
2015     Institute for Clinical Effectiveness and Health Policy (IECS) [Pharmacogenetic test (Neurofarmagen®) to assess the potential response to drugs and adverse effects in patients with neuropsychiatric disorders]
2015     Gesundheit Osterreich GmbH (GOeG) [Pharmaceutical stroke prevention in atrial fibrillation]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Voxelotor (haemolytic anaemia in sickle cell disease, monotherapy or combination with hydroxycarbamide, ≥ 12 years)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Vosoritide (achondroplasia, ≥ 2 years)]
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Voretigene Neparvovec]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Voretigene Neparvovec (reassessment after the deadline: inherited retinal dystrophy)]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Volanesorsen]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Valoctocogene roxaparvovec (severe haemophilia A)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Tisagenlecleucel (reassessment after the deadline: B-cell acute lymphoblastic leukaemia (ALL), relapsed/ refractory, 0 ≤ 25 years)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Tisagenlecleucel (reassessment after the deadline (diffuse large B-cell lymphoma, (DLBCL))]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Tisagenlecleucel (reassessment after expiry: diffuse large B-cell lymphoma)]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Tisagenlecleucel (Reassessment after Expiry: B-cell Acute Lymphoblastic Leukaemia)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Tisagenlecleucel (new therapeutic indication: follicular lymphoma, pretreated patients)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Tebentafusp (uveal melanoma, HLA-A*02:01-positive)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Talquetamab (multiple myeloma, at least 3 prior therapies)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Tagraxofusp (blastic plasmacytoid dendritic cell neoplasm, first-line)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Tafasitamab (diffuse large B-cell lymphoma (DLBCL), combination with lenalidomide)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Sutimlimab (cold agglutinin disease)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Somatrogon (growth disturbance due to growth hormone deficiency, ≥ 3 to < 18 years]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Setmelanotide (obesity and control of hunger, POMC, PCSK1 or LEPR-deficiency obesity, ≥ 6 years)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Setmelanotide (new therapeutic indication: obesity and control of hunger, Bardet-Biedl syndrome, ≥ 6 years)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Selumetinib (neurofibromatosis (≥ 3 to < 18 years, type 1))]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Sebelipase alfa (reassessment after expiry of the deadline (lysosomal acid lipase deficiency))]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Satralizumab (neuromyelitis optica spectrum disorders, anti-aquaporin-4IgG seropositive, ≥ 12 years)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Ripretinib (gastrointestinal stromal tumours (GIST), ≥ 3 prior therapies)]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Ponatinib (Reassessment after the Deadline: Chronic Myeloid Leukaemia)]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Ponatinib (Reassessment after the Deadline: Acute Lymphoblastic Leukaemia)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Polatuzumab Vedotin (new therapeutic indication: diffuse large B-cell lymphoma (DLBCL), combination with rituximab, cyclophosphamide, doxorubicin and prednisone (R-CHP))]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Polatuzumab Vedotin (Diffuse Large B-Cell Lymphoma, Combination with Bendamustine and Rituximab)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Pemigatinib (cholangiocarcinoma with FGFR2 fusion or FGFR2 rearrangement, after at least one prior therapy)]
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Pegvaliase]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Pegcetacoplan (paroxysmal nocturnal haemoglobinuria, pretreated patients)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Osilodrostat (Endogenous Cushing’s Syndrome)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Mosunetuzumab (follicular lymphoma, after ≥ 2 prior therapies)]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Mogamulizumab (Mycosis Fungoides, Sézary Syndrome)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Migalastat (new therapeutic indication: Fabry disease, 12 to < 16 years)]
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Mexiletine]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Luspatercept (β-thalassaemia)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Luspatercept (Myelodysplastic Syndrome (MDS))]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Lumasiran (Hyperoxaluria)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Lonapegsomatropin (growth failure due to growth hormone deficiency, ≥ 3 to < 18 years)]
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Ixazomib]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Ixazomib (reassessment after the deadline: multiple myeloma, at least 1 prior therapy, combination with lenalidomide and dexamethasone)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Ivosidenib (cholangiocarcinoma with IDH1 R132 mutation, after at least 1 prior therapy)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Ivacaftor/Tezacaftor/Elexacaftor (exceeding the € 50 million limit, cystic fibrosis, combination treatment with Ivacaftor in patients 12 years and older (homozygous for F508del mutation))]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Ivacaftor/Tezacaftor/Elexacaftor (Exceeding the € 50 Million Limit, Cystic Fibrosis, Combination Treatment with Ivacaftor in Patients 12 Years and Older (Heterozygous for F508del and MF Mutation))]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Imlifidase (desensitisation in kidney transplantation)]
2016     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Idebenone]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Idebenone (reassessment after the deadline: Leber's Hereditary Optic Neuropathy)]
2019     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Glycerol phenylbutyrate (New Therapeutic Indication: Urea cycle disorders in infants aged 0 to < 2 months)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Glucarpidase (reduction of toxic plasma methotrexate concentrations; aged 28 days and older)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Glasdegib (acute myeloid leukaemia (AML), combination with cytarabine (LDAC))]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Givosiran (acute hepatic porphyria, ≥ 12 years)]
2020     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Gilteritinib (Relapsed or Refractory Acute Myeloid Leukaemia with an FLT3 Mutation)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Fenfluramine (new therapeutic indication: Lennox-Gastaut syndrome, add-on therapy, ≥ 2 years)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Fenfluramine (Dravet syndrome, ≥ 2 years)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Fenfluramine (Dravet syndrome, ≥ 2 years)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Fedratinib (myelofibrosis)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Etranacogene dezaparvovec (haemophilia B)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Eladocagene exuparvovec (Aromatic-L-amino acid decarboxylase (AADC) deficiency, ≥ 18 months)]
2023     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Efgartigimod alfa (Myasthenia Gravis, AChR-antibody+)]
2022     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Delamanid (repeal of the exemption: pulmonary multi-drug resistant tuberculosis, ≥ 10 kg)]
2021     The Federal Joint Committee (G-BA) [Pharmaceutical Directive/Annex XII: Crizanlizumab (repeal of the resolution of 20 May 2021)]