ADHD
-
Lisdexamfetamine
- Molindone
ALL
-
Blinatumomab
- Blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with high-risk first relapsed Philadelphia chromosome negative CD19 positive B-precursor ALL as part of the consolidation therapy.
- Blincyto is indicated as monotherapy for the treatment of adults with CD19 positive relapsed or refractory B-precursor acute lymphoblastic leukaemia (ALL). Patients with Philadelphia chromosome positive B-precursor ALL should have failed treatment with at least 2 tyrosine kinase inhibitors (TKIs) and have no alternative treatment options.
-
Dasatinib
- Geïndiceerd voor de behandeling van volwassen patiënten met: nieuw gediagnosticeerde Philadelphiachromosoom-positieve (Ph+) chronische myeloïde leukemie (CML) in de chronische fase. CML in de chronische, acceleratie- of blastaire fase, die resistent of intolerant zijn voor eerder toegediende geneesmiddelen inclusief imatinib. Ph+ acute lymfoblastaire leukemie (ALL) en lymfoïde blasten CML die resistent of intolerant zijn voor eerder toegediende geneesmiddelen. Ook geïndiceerd voor de behandeling van pediatrische patiënten met: nieuw gediagnosticeerde Ph+ CML in de chronische fase (Ph+ CML-CP) of met Ph+ CML-CP die resistent of intolerant zijn voor eerder toegediende geneesmiddelen waaronder imatinib. Nieuw gediagnosticeerde Ph+ ALL in combinatie met chemotherapie.
- Geïndiceerd voor de behandeling van volwassen patiënten met: nieuw gediagnosticeerde Philadelphiachromosoom-positieve (Ph+) chronische myeloïde leukemie (CML) in de chronische fase. CML in de chronische, acceleratie- of blastaire fase, die resistent of intolerant zijn voor eerder toegediende geneesmiddelen inclusief imatinib. Ph+ acute lymfoblastaire leukemie (ALL) en lymfoïde blasten CML die resistent of intolerant zijn voor eerder toegediende geneesmiddelen. Ook geïndiceerd voor de behandeling van pediatrische patiënten met: nieuw gediagnosticeerde Ph+ CML in de chronische fase (Ph+ CML-CP) of met Ph+ CML-CP die resistent of intolerant zijn voor eerder toegediende geneesmiddelen waaronder imatinib. Nieuw gediagnosticeerde Ph+ ALL in combinatie met chemotherapie.
-
autologous anti-CD19-transduced CD3+ cells
ALS
-
Arimoclomol
AML/MDS
-
Arseentrioxide
- Geïndiceerd voor het induceren van remissie en consolidatie bij volwassen patiënten met: 1) nieuw gediagnosticeerde acute promyelocytaire leukemie (APL) met laag tot middelmatig risico (aantal witte bloedcellen ≤ 10 x 103/μl) in combinatie met all-trans-retinoïnezuur (ATRA), 2) recidiverende/refractaire acute promyelocytaire leukemie (APL) (tijdens een eerdere behandeling moet een retinoïde stof zijn toegediend en chemotherapie hebben plaatsgehad), gekenmerkt door de aanwezigheid van de translocatie t(15;17) en/of de aanwezigheid van het gen promyeolocitaire-leukemie-/retinoïnezuurreceptor-alfa (PML/RAR-alfa).
- Geïndiceerd voor het induceren van remissie en consolidatie bij volwassen patiënten met: 1) nieuw gediagnosticeerde acute promyelocytaire leukemie (APL) met laag tot middelmatig risico (aantal witte bloedcellen ≤ 10 x 103/μl) in combinatie met all-trans-retinoïnezuur (ATRA), 2) recidiverende/refractaire acute promyelocytaire leukemie (APL) (tijdens een eerdere behandeling moet een retinoïde stof zijn toegediend en chemotherapie hebben plaatsgehad), gekenmerkt door de aanwezigheid van de translocatie t(15;17) en/of de aanwezigheid van het gen promyeolocitaire-leukemie-/retinoïnezuurreceptor-alfa (PML/RAR-alfa).
-
Azacitidine
- Eprenetapopt
-
Gilteritinib
- Glasdegib
- Guadecitabine
- Idasanutlin
- Imetelstat
- Iomab-B
- Pevonedistat
- Sapacitabine
-
Venetoclax
Allergie
- Adrenaline
- Arachis hypogaea (pinda) allergenen (capsule)
- Arachis hypogaea (pinda) allergenen (pleister)
- Olopatadine / mometasone
Alvleesklierkanker
-
Eryaspase (Asparaginase)
-
Olaparib
Antitrombotische medicatie
-
Apixaban
- Dabigatran G
- Dabigatran etexilate IND
-
Ravulizumab
-
Rivaroxaban
Astma
-
Beclometason/formoterol/glycopyrronium
- Budesonide / formoterol IND
-
Dupilumab
-
Fluticasone furoate / umeclidinium / vilanterol
- Indacaterol acetate/glycopyrronium bromide/mometasone furoate
- Indacaterol acetate/mometasone furoate
-
Masitinib
-
Omalizumab
- Aanvullende behandeling om de astmacontrole te verbeteren bij patiënten met ernstig persistent allergisch astma. Ook voor de behandeling van chronische idiopathische urticaria.
- Aanvullende behandeling om de astmacontrole te verbeteren bij patiënten met ernstig persistent allergisch astma.
- Aanvullende behandeling om de astmacontrole te verbeteren bij patiënten met ernstig persistent allergisch astma.
-
Tezepelumab
Baarmoederhalskanker
-
Cemiplimab
-
Lifileucel
Bacteriele infecties
- Amoxicilline / omeprazol / rifabutin
-
Bedaquiline
-
Ceftaroline fosamil
-
Ceftazidime / avibactam
- Treatment of patients with bacteraemia that occurs in association with, or is suspected to be associated with, the currently approved indications for complicated intra-abdominal infection (cIAI), complicated urinary tract infection (cUTI) and hospital-acquired pneumonia, including ventilator-associated pneumonia.
- Zavicefta is indicated in adults and children aged 3 months and older and adolescents for the treatment of the following infections in adults with Complicated intra-abdominal infection (cIAI), Complicated urinary tract infection (cUTI), including pyelonephritis, Hospital-acquired pneumonia (HAP), including ventilator associated pneumonia (VAP).
- Ceftobiprole
-
Delafloxacin
-
Delamanid
- Iclaprim
-
Imipenem / cilastatin / relebactam
- Recarbrio is indicated for the treatment of infections due to aerobic Gram-negative organisms in adults with limited treatment options.
- Treatment of hospital-acquired pneumonia (HAP), including ventilator associated pneumonia (VAP), in adults. Treatment of bacteraemia that occurs in association with, or is suspected to be associated with HAP or VAP, in adults.
- Lefamulin
- Liposomaal amikacine
- Obiltoxaximab
- Ozenoxacine
-
Pretomanid
- SER 109
- Tebipenem
-
Tedizolid
Bipolaire stoornis
Blaaskanker
-
Atezolizumab
-
Avelumab
-
Durvalumab
-
Enfortumab vedotin
-
Erdafitinib
-
Nivolumab
- Oportuzumab monatox
Borstkanker
-
Abemaciclib
-
Alpelisib
-
Atezolizumab
- Balixafortide
- Efbemalenograstim alfa
- Margetuximab
-
Neratinib
-
Olaparib
-
Paclitaxel
-
Pembrolizumab
- Extension of indication for Keytruda to include in combination with chemotherapy, treatment of locally recurrent unresectable or metastatic triple negative breast cancer in adults whose tumours express PD L1 with a CPS ≥ 10 and who have not received prior chemotherapy for metastatic disease.
- Triple Negative Breast Cancer - Neoadjuvant and adjuvant.
- Pertuzumab / trastuzumab
-
Sacituzumab govitecan
- Tesetaxel
-
Trastuzumab deruxtecan
- Patients with HER2 low, unresectable, and/or metastatic breast cancer previously treated with 1-2 prior lines of chemotherapy in the metastatic setting and has progressed on, and would no longer benefit from, endocrine therapy.
- Treatment of adult patients with Human Epidermal Growth Factor Receptor 2 (HER2)-Positive, Unresectable and/or Metastatic Breast Cancer Previously Treated With Trastuzumab and Taxane 2L.
- Enhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic HER2 positive breast cancer who have received two or more prior anti HER2 based regimens.
- Trastuzumab duocarmazine
-
Trastuzumab emtansine
-
Tucatinib
Borstvlieskanker
CLL
-
Acalabrutinib
- Calquence as monotherapy is indicated for the treatment of adult patients with relapsed/refractory CLL (chronic lymphocytic leukemia).
- Calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (CLL).
- Duvelisib
-
Ibrutinib
- Extension of indication in chronic lymphocytic leukaemia (CLL) to add combination with rituximab as follows; Ibrutinib in combination with rituximab or obinutuzumab for the treatment of adult patients with previously untreated CLL (Young and Fit).
- Extension of indication to the existing chronic lymphocytic leukaemia (CLL) indication to include combination use with obinutuzumab for the treatment of adult patients with previously untreated CLL.
- Moxetumomab pasudotox
-
Ublituximab
-
Venetoclax
-
ibrutinib
COPD
-
Beclometason/formoterol/glycopyrronium
-
Formoterol / glycopyronium / budesonide
- Revefenacin
Chronische immuunziekten, overig
-
Anakinra
-
Baricitinib
- Belatacept IND
-
Belimumab
-
Berotralstat
- Elobixibat
- Forigerimod
-
Icatibant
-
Imlifidase
- MDR-101
- Mavorixafor
- RP-L201
- Teprasiran
- Teprotumumab
- Triamcinolone
- Voclosporin
Darmkanker
Darmziekten
-
Adalimumab
-
Etrolizumab
-
Filgotinib
-
Mirikizumab
-
Ozanimod
-
Remestemcel-L
-
Risankizumab
-
Tenapanor
-
Upadacitinib
Dementie
- Aducanumab
-
Leuco-methylthioninium
Depressie
- Brexanolone
- Bupropion/dextromethorphan
-
Esketamine
- Spravato, in combination with a SSRI or SNRI, is indicated for adults with treatment-resistant major depressive disorder, who have not responded to at least two different treatments with antidepressants in the current moderate to severe depressive episode.
- Extension of indication to include a new indication for SPRAVATO® (esketamine nasal spray) co-administered with oral antidepressant therapy in adults with a moderate to severe episode of Major Depressive Disorder (MDD), as acute short term treatment, for the rapid reduction of depressive symptoms, which according to clinical judgement constitute a psychiatric emergency.
- Zuranolone
Diabetes
- Bexagliflozine
-
Dapagliflozine
-
Dasiglucagon
-
Exenatide
- Finerenone
-
Glucagon
-
Insulin aspart
- Insulin lispro (ultra rapid formulation)
- Polyethylene glycol loxenatide
- Reparixin
-
Sotagliflozine
- Teplizumab
-
Tirzepatide
Duchenne
Eierstokkanker
-
Niraparib
-
Olaparib
-
Veliparib
Epilepsie
- Brivaracetam IND
-
Cannabidiol
- Cenobamate
-
Fenfluramine
- Ganaxolone
- Lacosamide IND
- Perampanel IND
Fungale infecties
-
Ibrexafungerp
-
Posaconazol
- Rezafungin
Gehooraandoeningen
HIV
- Atazanavir / cobicistat
- Cabotegravir
- Etravirine IND
- Fostemsavir
-
Lenacapavir
Hart- en vaatziekten
Hematologie, overig
-
Ibrutinib
-
Zanubrutinib
Hemostase bevorderende medicatie
Hersenkanker
Hodgkin lymfoom
Hoofd- en halskanker
-
Durvalumab
-
Leukocyte interleukin
-
Pembrolizumab
Hoofdpijn
-
Eptinezumab
- Erenumab
-
Fremanezumab
-
Galcanezumab
- Lasmiditan
- Meloxicam/rizatriptan
-
Rimegepant
Hormonale aandoeningen
- Drospirenon / estetrol, monohydraat
- Levoketoconazole
-
Linzagolix
- Lonapegsomatropin
-
Octreotide
- Osilodrostat
-
Relugolix
- Relugolix / estradiol / norethisteronen
-
Somapacitan
-
Somatrogon
-
Tenapanor
Huidkanker
-
Atezolizumab
-
Cemiplimab
- Libtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (laBCC or mBCC) who have progressed on or are intolerant to a hedgehog pathway inhibitor (HHI).
- Monotherapy treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma who are not candidates for curative surgery or curative radiation.
- Darleukin fibromun
-
Lifileucel
- Relatlimab
- Seviprotimut-L
- Tavokinogene telseplasmid
Huidziekten
-
Abrocitinib
- Beremagene geperpavec
- Berkenschorsextract
-
Bimekizumab
- Clascoterone
- Crisaborole
- Difelikefalin
-
Dupilumab
- Glycopyrronium tosylate
-
Lebrikizumab
- Nemolizumab
- Regenerative Skin Tissue
-
Risankizumab
-
Ruxolitinib
-
Secukinumab
-
Spesolimab
-
Tapinarof
- Tirbanibulin
-
Tralokinumab
-
Upadacitinib
Infectieziekten, overig
Leukemie
Leverkanker
-
Atezolizumab
-
Durvalumab
-
Pembrolizumab
-
Pemigatinib
-
Tremelimumab
Leverziekten
- Cenicriviroc
- Givosiran
-
Maralixibat
-
Obeticholic acid
-
Odevixibat
- Seladelpar
Lipidenverlagende medicatie
- Bempedoic acid
-
Bempedoic acid / ezetimibe
-
Evinacumab
-
Evolocumab
-
Inclisiran
Long, overig
-
Benralizumab
- Gefapixant
-
Mepolizumab
-
Nintedanib
-
Pirfenidone
Longkanker
-
Amivantamab
-
Atezolizumab
-
Avelumab
-
Brigatinib
- Capmatinib
-
Cemiplimab
- Cemiplimab wordt onderzocht als eerstelijns behandeling in combinatie met chemotherapie voor volwassen patiënten met lokaal gevorderd of gemetastaseerde plaveiselcel en niet-plaveiselcel NSCLC (stadium IIIB/C-IV) onafhankelijk van PD-L1 expressie.
- Libtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (NSCLC) expressing PD-L1 (in ≥ 50% tumour cells), with no EGFR, ALK or ROS1 aberrations, who have locally advanced NSCLC who are not candidates for definitive chemoradiation, or metastatic NSCLC.
-
Durvalumab
- Non-small cell lung cancer (NSCLC) stage IV, in combination with tremelimumab and chemo,1L.
- 1L advanced NSCLC
- Non-small cell lung cancer (NSCLC) stage IV, in combination with chemo, 1L.
- Lokaal gevorderd, niet-resectabel NSCLC (stadium III)
- Completely resected NSCLC
- Imfinzi in combination with etoposide and either carboplatin or cisplatin is indicated for the first-line treatment of adults with extensive-stage small cell lung cancer (ES-SCLC).
- Ensartinib
-
Entrectinib
-
Lorlatinib
-
Lurbinectedin
-
Nivolumab
-
Osimertinib
-
Pralsetinib
-
Selpercatinib
- Sotorasib
- Tedopi
- Tepotinib
- Trilaciclib
Lymfeklierkanker
Maagkanker
-
Avapritinib
-
Nivolumab
- Ripretinib
- Rivoceranib
-
Trastuzumab deruxtecan
Multipel Myeloom
-
Belantamab mafodotin
- Blenrep is indicated as monotherapy for the treatment of multiple myeloma in adult patients, who have received at least four prior therapies and whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and an anti-CD38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.
- Multiple Myeloma 3L
-
Carfilzomib
-
Daratumumab
- Extension of indication to extend the existing therapeutic indication for daratumumab in combination with bortezomib, thalidomide and dexamethasone for the treatment of adult patients with newly diagnosed multiple myeloma who are eligible for autologous stem cell transplant (ASCT).
- Multipel myeloom frontline behandeling in cpmbinatie met VRd voor patiënten die niet in aanmerking komen voor een ASCT.
- Smouldering multipel myeloom.
- Subcutaneous formulation indicates for Relapsed or Refractory Multiple Myeloma.
- Darzalex is indicated in combination with cyclophosphamide, bortezomib and dexamethasone for the treatment of adult patients with newly diagnosed systemic light chain (AL) amyloidosis.
- In combination with pomalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received one prior therapy containing a proteasome inhibitor and lenalidomide and were lenalidomide-refractory, or who have received at least two prior therapies that included lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or after the last therapy.
- Extension of indication to extend the existing therapeutic indication for daratumumab in combination with lenalidomide and dexamethasone (Rd) for the treatment of adult patients with newly diagnosed multiple myeloma who are ineligible for autologous stem cell transplant (ASCT).
-
Idecabtagene vicleucel
-
Isatuximab
- Sarclisa is indicated in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.
- In Combination With Bortezomib, Lenalidomide and Dexamethasone (Isa VRd) in Patients With Newly Diagnosed Multiple Myeloma (NDMM) Not Eligible for Transplant.
- JNJ-4528
-
Lenalidomide
-
Pomalidomide
-
Selinexor
- Extension of indication for Nexpovio in combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.
- Nexpovio is indicated in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-CD38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.
Multiple sclerose
- Diroximel fumarate
- Fampridine G
-
Fingolimod
-
Masitinib
-
Natalizumab
- Ofatumumab
- Ponesimod
- Siponimod
-
Teriflunomide
Myeloproliferatieve aandoeningen
Neuro-endocriene kanker
-
Selumetinib
- Surufatinib
Neurologie, overig
- Cannabidiol gel/intradermaal
- Eladocagene exuparvovec
-
Inebilizumab
- Remimazolam
- Ronopterin
-
Satralizumab
-
Tiratricol
Nierkanker
-
Avelumab
-
Cabozantinib
-
Lenvatinib
-
Pembrolizumab
- Tivozanib IND
Non-hodgkin lymfoom agressief
-
Axicabtagene ciloleucel
-
Ibrutinib
-
Lisocabtagene maraleucel
-
Polatuzumab vedotin
-
Tafasitamab
- Tagraxofusp
-
Zanubrutinib
Non-hodgkin lymfoom indolent
-
Axicabtagene ciloleucel
- Copanlisib
-
Ibrutinib
- Umbralisib
Onbekend
Oncologie, overig
- 131I-omburtamab
-
Dostarlimab
-
Durvalumab
-
Entrectinib
- Glucarpidase
-
Ivosidenib
- Larotrectinib
-
Lenvatinib
- Lipegfilgrastim IND
- NY-ESO-1 autologous engineered TCR-T cells
-
Nivolumab
- Extension of indication to include adjuvant treatment of adult patients with resected oesophageal, or gastro-oesophageal junction cancer who have residual pathologic disease following prior neoadjuvant chemoradiotherapy for OPDIVO.
- Opdivo as monotherapy is indicated for the treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma after prior fluoropyrimidine- and platinum-based combination chemotherapy.
-
Pembrolizumab
- Women With Persistent, Recurrent, or Metastatic Cervical Cancer (1L).
- Extension of indication to include pembrolizumab in combination with lenvatinib for the treatment of advanced endometrial carcinoma in adults who have disease progression following prior systemic therapy in any setting and who are not candidates for curative surgery or radiation.
- Keytruda, in combination with platinum and fluoropyrimidine based chemotherapy, is indicated for the first-line treatment of patients with locally advanced unresectable or metastatic carcinoma of the oesophagus or HER-2 negative gastroesophageal junction adenocarcinoma in adults whose tumours express PD‑L1 with a CPS ≥ 10.
- Keytruda as monotherapy is indicated for the first‑line treatment of metastatic microsatellite instability‑high (MSI‑H) or mismatch repair deficient (dMMR) colorectal cancer in adults.
-
Retifanlimab
-
Selinexor
- Sodium thiosulfate
Oogaandoeningen
-
Aflibercept
- Aganirsen
- Avacincaptad pegol
- Bevacizumab-vikg
-
Brolucizumab
-
Faricimab
- Latanoprostene bunod
- Lenadogene nolparvovec
- Netarsudil / latanoprost
- Perfluorohexyloctane
- Polihexanide
-
Ranibizumab
-
Reproxalap
- Sepofarsen
- Timrepigene emparvovec
- Voretigene neparvovec
Overige medicatie hart-en vaatziekten
- Allogenic immunomodulatory progenitor cells
- Apabetalon
-
Dapagliflozine
- Emiplacel
-
Empagliflozine
- Icosapent ethyl
- Omecamtiv mecarbil
-
Rilonacept
- Tafamidis IND
-
Ticagrelor
- Extension of indication to include, in co-administration with acetylsalicylic acid (ASA), the prevention of stroke in adult patients with acute ischaemic stroke or transient ischaemic attack (TIA) in the previous 24 hours.
- Extension of indication to include, in co administration with acetylsalicylic acid (ASA), the prevention of atherothrombotic events in adult patients with coronary artery disease (CAD) and type 2 diabetes mellitus (T2DM) without a history of myocardial infarction who have undergone percutaneous coronary intervention (PCI).
- Udenafil
-
Valsartan / sacubitril
-
Vericiguat
Overige niet-oncologische hematologische medicatie
- Avatrombopag
-
Betibeglogene autotemcel
- Zynteglo is geïndiceerd voor gebruik bij patiënten in de leeftijd van 12 jaar en ouder met transfusie-afhankelijke β-thalassemie (transfusion-dependent β-thalassaemia - TDT) die geen β0/β0-genotype hebben, voor wie transplantatie van hematopoëtische stamcellen (HSC) gepast is, maar geen humaan leukocytenantigeen (HLA)-compatibele gerelateerde HSC-donor beschikbaar is.
- Behandeling van patiënten jonger dan 12 jaar met transfusie-afhankelijke β-thalassemie (TDT) die geen β0/β0-genotype hebben en voor wie hematopoïetische stamceltransplantatie (HSC) gepast is, maar voor wie geen humaan leukocyt antigeen (HLA)-compatibele verwante HSC-donor beschikbaar is.
- Behandeling van patiënten met transfusie-afhankelijke β-thalassemie (TDT) die een β0 mutatie op beide allelen van het β-globuline (HBB) hebben, en voor wie hematopoïetische stamceltransplantatie (HSC) gepast is, maar voor wie geen humaan leukocyt antigeen (HLA)-compatibele verwante HSC-donor beschikbaar is
- Crizanlizumab
- Daprodustat
-
Deferasirox
-
Eculizumab
-
Efgartigimod
- Ferumoxytol
-
Hydroxycarbamide
-
Luspatercept
-
Mepolizumab
-
Mitapivat
-
Pegcetacoplan
- RP-L102
-
Ravulizumab
- Treatment of adult patients with paroxysmal nocturnal haemoglobinuria (PNH) in patients with haemolysis with clinical symptom(s) indicative of high disease activity and in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months.
- Extension of indication to include treatment of paediatric patients with paroxysmal nocturnal haemoglobinuria (PNH) for Ultomiris.
-
Romiplostim
- Roxadustat
- Thrombomodulin alfa
- Vadadustat
- Voxelotor
Parkinson
- Amantadine
- Apomorphine
- Istradefylline
-
Levodopa / carbidopa
Pijn
-
Bupivacaine
- Bupivacaine / meloxicam
- Fasinumab
- Lidocaïne
- Neridronic Acid
- SDN037
-
Tanezumab
Prostaatkanker
- 177Lu-PSMA-617 IND
-
Abiraterone
- Geïndiceerd met prednison of prednisolon voor: - de behandeling van nieuw gediagnosticeerde hoog-risico gemetastaseerde hormoongevoelige prostaatkanker (mHSPC) bij volwassen mannen, in combinatie met androgeendeprivatietherapie (ADT); - de behandeling van gemetastaseerde castratieresistente prostaatkanker (mCRPC) bij volwassen mannen die asymptomatisch of licht symptomatisch zijn na falen van androgeendeprivatietherapie en voor wie behandeling met chemotherapie nog niet klinisch geïndiceerd is ; - de behandeling van mCRPC bij volwassen mannen bij wie de ziekte progressief was tijdens of na een chemotherapieschema op basis van docetaxel.
- Geïndiceerd met prednison of prednisolon voor: - de behandeling van nieuw gediagnosticeerde hoog-risico gemetastaseerde hormoongevoelige prostaatkanker (mHSPC) bij volwassen mannen, in combinatie met androgeendeprivatietherapie (ADT); - de behandeling van gemetastaseerde castratieresistente prostaatkanker (mCRPC) bij volwassen mannen die asymptomatisch of licht symptomatisch zijn na falen van androgeendeprivatietherapie en voor wie behandeling met chemotherapie nog niet klinisch geïndiceerd is ; - de behandeling van mCRPC bij volwassen mannen bij wie de ziekte progressief was tijdens of na een chemotherapieschema op basis van docetaxel.
- Geïndiceerd met prednison of prednisolon voor: - de behandeling van nieuw gediagnosticeerde hoog-risico gemetastaseerde hormoongevoelige prostaatkanker (mHSPC) bij volwassen mannen, in combinatie met androgeendeprivatietherapie (ADT); - de behandeling van gemetastaseerde castratieresistente prostaatkanker (mCRPC) bij volwassen mannen die asymptomatisch of licht symptomatisch zijn na falen van androgeendeprivatietherapie en voor wie behandeling met chemotherapie nog niet klinisch geïndiceerd is ; - de behandeling van mCRPC bij volwassen mannen bij wie de ziekte progressief was tijdens of na een chemotherapieschema op basis van docetaxel.
- Abiraterone / apalutamide
-
Apalutamide
-
Cabazitaxel
- DCVAC
-
Darolutamide
-
Enzalutamide
-
Masitinib
-
Olaparib
- Monotherapy for the treatment of adult patients with metastatic castration-resistant prostate cancer and BRCA1/2-mutations (germline and/or somatic) who have progressed following prior therapy that included a new hormonal agent. (only BRCA mutations included in the indication).
- Treatment in combination with abiraterone acetate in patients with metastatic Castration-resistant Prostate Cancer (mCRPC) who have not received prior chemotherapy or new hormonal agents (NHAs) for metastatic castration-resistant prostate cancer (mCRPC) (first-line setting).
-
Relugolix
Psychiatrie, overig
-
Dexmedetomidine
Reuma
-
Anifrolumab
-
Guselkumab
- Olokizumab
-
Risankizumab
-
Sarilumab
-
Tocilizumab
-
Tofacitinib
-
Upadacitinib
- Rinvoq is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more DMARDs. Rinvoq may be used as monotherapy or in combination with methotrexate.
- Rinvoq is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy.
SMA
-
Onasemnogene abeparvovec
-
Risdiplam
Schildklierkanker
-
Selpercatinib
Schizofrenie, psychose
-
Lurasidone
- Olanzapine / samidorphan
Slaapstoornissen
- Daridorexant
- JZP-258
- Lemborexant
-
Natriumoxybaat
- Natriumoxybaat controlled release
-
Pitolisant
-
Tasimelteon
Spierziekten
- Bidridistrogene xeboparvovec
-
Sugammadex
Spierziekten, overig
Stamceltransplantaties
- Inolimomab
- Itacitinib
- Motixafortide
- Narsoplimab
- Omidubicel
-
Remestemcel-L
- Rimiducid
- Rivogenlecleucel
-
Ruxolitinib
- Tabelecleucel
- Thiotepa G
-
autologous anti-CD19-transduced CD3+ cells
Stofwisseling en Endocrinologie, overig
- Autologous human chondrocytes in vitro expanded
-
Burosumab
-
Dapagliflozine
- Diazoxide choline (controlled-release tablet)
-
Elamipretide
- Fexapotide
-
Liraglutide
- Lumasiran
- Nolasiban
- Romosozumab
-
Semaglutide
-
Setmelanotide
- Sofpironium bromide
- Spheroids of human autologous matrix-associated chondrocytes IND
-
Vosoritide
Stofwisselingsziekten
-
Arimoclomol
- Autologous CD34+ cell enriched population that contains hematopoietic stem and progenitor cells transduced ex vivo using a lentiviral vector encoding the human arylsulfatase A gene
- Avalglucosidase alfa
- Betaine G
- Cipaglucosidase alfa / Miglustat
- Elivaldogene autotemcel
-
Hydrocortison
- Kaliumcitraat / kaliumwaterstofcarbonaat
-
Lonafarnib
-
Migalastat
- Olipudase alfa
- Pegunigalsidase alfa
-
Pegvaliase
- Reloxaliase
- Sapropterin G
- Sodium zirconium cyclosilicate
- Trientine
- Triheptanoin
- Veverimer
-
Volanesorsen
Taaislijmziekte
- Bamocaftor / tezacaftor / ivacaftor
-
Elexacaftor / tezacaftor / ivacaftor
- Kaftrio is indicated in a combination regimen with ivacaftor 150mg tablets for the treatment of cystic fibrosis (CF) in patients aged 12 years and older who have at least one F508del mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene
- Uitbreiding van Kaftrio in combinatie met ivacaftor voor patienten met tenminste één F508del mutatie naar de leeftijd vanaf 6 jaar (uitbreiding voor 6 tot 11 jarigen)
-
Ivacaftor
-
Lumacaftor / ivacaftor
-
Tezacaftor / ivacaftor
Virale infecties, overig
- APN01
-
Baloxavir marboxil
- Bamlanivimab/ etesevimab
-
Baricitinib
-
Bulevirtide
- Casirivimab/imdevimab
-
Dapagliflozine
- Elbasvir / grazoprevir IND
-
Glecaprevir / pibrentasvir
-
Lonafarnib
- Maribavir
-
Nirsevimab
- Regdanvimab
-
Remdesivir
- Veklury is geïndiceerd voor de behandeling van coronavirus disease 2019 (COVID-19) bij volwassenen en jongeren (vanaf 12 jaar die minstens 40kg wegen) met pneumonie die aanvullende zuurstof nodig hebben.
- Extension of indication to include treatment of adults with pneumonia not requiring supplemental oxygen (moderate COVID-19).
- Sotrovimab
- Tecovirimat
- Zanamivir