| 21041 |
Daratumumab |
Darzalex® in combination with cyclophosphamide, bortezomib and dexamethasone |
For the treatment of adult patients with newly diagnosed systemic light chain amyloidosis. |
NCPE Assessment Process Complete |
5th June 2024 |
 |
| 22039 |
Daratumumab |
Darzalex® |
In combination with lenalidomide (Revlimid®) and dexamethasone for the treatment of adult patients with newly diagnosed multiple myeloma who are ineligible for autologous stem cell transplant |
NCPE Assessment Process Complete |
5th June 2024 |
|
| 20022 |
Darolutamide |
Nubeqa® |
For the treatment of adult men with non-metastatic castration resistant prostate cancer (nmCRPC) who are at high risk of developing metastatic disease. |
NCPE Assessment Process Complete |
10th September 2021 |
|
| - |
Darunavir & cobicistat |
Rezolsta® |
Indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus-1 (HIV-1) infection in adults aged 18 years or older. |
Rapid review complete |
8th January 2015 |
|
| - |
Darunavir/ cobicistat/ emtricitabine/ tenofovir alafenamide |
Symtuza® |
For the treatment of HIV-1 in adults and adolescents. |
Rapid review complete |
26th October 2017 |
|
| - |
Darvadstrocel |
Alofisel® |
For the treatment of complex perianal fistulae in adult patients with non-active/ mildly active luminal Crohn’s Disease when fistulae have shown an inadequate response to at least one conventional or biologic therapy and should be used after conditioning of fistula. |
NCPE Assessment Process Complete |
24th September 2019 |
|
| - |
Decitabine |
Dacogen® |
For AML in patients who are >65yrs who are not candidates for standard induction therapy |
Rapid review complete |
21st December 2012 |
|
| 22019 |
Defatted powder of Arachis hypogaea L., semen (peanuts) |
Palforzia® |
For the treatment of patients aged 4 to 17 years with a confirmed diagnosis of peanut allergy. Palforzia® may be continued in patients 18 years of age and older. Palforzia® should be used in conjunction with a peanut-avoidant diet. |
NCPE Assessment Process Complete |
29th November 2023 |
|
| - |
Defibrotide |
Defitelio® |
Indicated in adults, children and infants (>1month) for the treatment of severe hepatic veno-occlusive disease (VOD) also known as sinusoidal obstruction syndrome (SOS) in haematopoietic stem-cell transplantation (HSCT) therapy |
Rapid review complete |
15th July 2014 |
|
| - |
Degarelin |
Firmagon® |
For the treatment of prostate cancer |
Rapid review complete |
15th October 2009 |
|
| 20038 |
Delafloxacin |
Quofenix® |
For the treatment of acute bacterial skin and skin structure infections (ABSSSI) in adults when it is considered inappropriate to use other antibacterial agents that are commonly recommended for the initial treatment of these infections. Consideration should be given to official guidance on the appropriate use of antibacterial agents. |
Rapid review complete |
19th November 2020 |
|
| - |
Delta-9-tetrahydrocannabinol/Cannabidiol, THC/CBD |
Sativex® |
Indicated as treatment for symptom improvement in adult patients with moderate to severe spasticity due to multiple sclerosis (MS) who have not responded adequately to other anti-spasticity medication and who demonstrate clinically significant improvement in spasticity related symptoms during an initial trial of therapy. |
NCPE Assessment Process Complete |
20th October 2023 |
|
| - |
Denosumab |
Prolia® |
For the Prevention of Osteoporotic Fractures in Postmenopausal Women |
NCPE Assessment Process Complete |
1st July 2010 |
|
| - |
Denosumab |
Xgeva® |
For the prevention of skeletal related events in adults with bone metastases from solid tumours in Ireland |
NCPE Assessment Process Complete |
8th December 2011 |
|
| 23030 |
Deucravacitinib |
Sotyktu® |
Deucravacitinib is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. |
Rapid Review Complete |
14th March 2024 |
|
| - |
Dexamethasone Intravitreal Implant |
Ozurdex® |
Treatment of macular oedema following Retinal Vein Occlusion |
NCPE Assessment Process Complete |
16th March 2012 |
|
| - |
Dexmedetomidine |
Dexdor® |
For the treatment of ICU adult patients requiring light to moderate sedation |
Rapid Review Complete |
6th September 2011 |
|
| - |
Diclofenac |
Itami® |
For the local symptomatic and short-term treatment (max. 7 days) of pain in acute strains, sprains or bruises of the extremities following blunt trauma e.g. sports injuries in adolescents aged from 16 years and adults |
Rapid Review Complete |
17th January 2019 |
|
| - |
Dienogest |
Visanne® |
For the Treatment of Endometriosis |
Rapid Review Complete |
4th October 2010 |
|
| 23001 |
Difelikefalin |
Kapruvia® |
For the treatment of moderate-to-severe pruritus associated with chronic kidney disease in adult patients on haemodialysis. |
NCPE Assessment Process Complete |
20th September 2024 |
|
| - |
Dimethyl fumarate |
Skilarence® |
For the treatment of moderate to severe plaque psoriasis in adults in need of systemic medicinal therapy. |
Rapid Review Complete |
6th February 2018 |
|
| - |
Dimethyl fumarate |
Tecfidera® |
For the treatment of adult patients with relapsing remitting multiple sclerosis (MS) |
NCPE Assessment Process Complete |
16th January 2015 |
|
| __ |
Dinutuximab beta |
Qarziba® |
For the treatment of high-risk neuroblastoma in patients ≥ 12 months, who have previously received induction chemotherapy and achieved at least a partial response, followed by myeloablative therapy and stem cell transplantation, as well as patients with a history of relapsed/refractory neuroblastoma, with or without residual disease. |
NCPE Assessment Process Complete |
22nd October 2018 |
|
| 21047 |
Diroximel fumarate |
Vumerity® |
For the treatment of adult patients with relapsing-remitting multiple sclerosis |
Rapid Review Complete |
16th December 2021 |
|
| - |
Dolutegravir |
Tivicay® |
In combination with other anti-retroviral medicinal products for the treatment of Human Immunodeficiency Virus (HIV) infected adults and adolescents above 12 years of age. |
Rapid Review Complete |
13th March 2014 |
|
| - |
Dolutegravir/lamivudine |
Dovato® |
For the treatment of Human Immunodeficiency Virus type 1 (HIV-1) infection in adults and adolescents above 12 years of age weighing at least 40kg, with no known or suspected resistance to the integrase inhibitor class, or lamivudine. |
Rapid Review Complete |
27th August 2019 |
|
| - |
Dolutegravir/Rilpivirine |
Juluca® |
For the treatment of HIV-1 infection in adults who are virologically-suppressed on a stable antiretroviral regimen for at least six months with no history of virological failure and no known or suspected resistance to any non-nucleoside reverse transcriptase inhibitor or integrase inhibitor. |
Rapid review complete |
12th July 2018 |
|
| - |
Doravirine |
Pifeltro® |
In combination with other antiretroviral medicinal products, for the treatment of adults infected with HIV-1 without past or present evidence of resistance to the non-nucleoside reverse transcriptase inhibitor (NNRTI) class. |
Rapid review complete |
16th January 2019 |
|
| - |
Doravirine/Lamivudine/Tenofovir Disoproxil Fumarate |
Delstrigo® |
For the treatment of adults infected with HIV-1 without past or present evidence of resistance to the non-nucleoside reverse transcriptase inhibitor (NNRTI) class, lamivudine or tenofovir |
Rapid review complete |
16th January 2019 |
|
| 24004 |
Dostarlimab |
Jemperli® |
Dostarlimab is indicated in combination with carboplatin and paclitaxel for the treatment of adult patients with mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H) primary advanced or recurrent endometrial cancer and who are candidates for systemic therapy. |
Full HTA submission received from Applicant |
22nd August 2024 |
|
| 21045 |
Dostarlimab |
Jemperli® |
Indicated as monotherapy for the treatment of adult patients with mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H) recurrent or advanced endometrial cancer that has progressed on or following prior treatment with a platinum-containing regimen. |
NCPE Assessment Process Complete |
27th March 2023 |
|
| 23052 |
Doxylamine/pyridoxine |
Cariban® |
Doxylamine/pyridoxine (Cariban®) is indicated for the symptomatic treatment of nausea and vomiting during pregnancy in adults who do not respond to conservative management. |
Rapid Review Complete |
14th March 2024 |
|
| - |
Doxylamine/pyridoxine |
Xonvea® |
For the treatment of nausea and vomiting of pregnancy in women who do not respond to conservative management. |
Rapid review complete |
15th August 2019 |
|
| - |
Dronedarone |
Multaq® |
__ |
Rapid review complete |
12th January 2010 |
|
| 22073 |
Drospirenone/estetrol monohydrate |
Drovelis® |
Drospirenone/estetrol monohydrate is indicated for oral contraception. |
Rapid Review Complete |
6th July 2023 |
|
| - |
Dulaglutide |
Trulicity® |
As monotherapy for the treatment of adult patients with T2DM when diet and exercise alone do not provide adequate glycaemic control in patients for whom the use of metformin is considered inappropriate due to intolerance or contraindications. Dulaglutide is indicated as an add-on therapy in combination with other glucose-lowering medicinal products including insulin, when these, together with diet and exercise, do not provide adequate glycaemic control. |
Rapid review complete |
29th April 2015 |
|
| 23047 |
Dupilumab |
Dupixent® |
Dupilumab (Dupixent®) is indicated for the treatment of adults and adolescents 12 years and older, weighing at least 40 kg, with eosinophilic oesophagitis (EoE) who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy. |
Rapid Review Complete |
7th September 2023 |
|
| 19056 |
Dupilumab |
Dupixent® |
For the treatment of moderate-to-severe atopic dermatitis in adolescents 12 years and older who are candidates for systemic therapy. |
Rapid review complete |
17th January 2020 |
|
| 23043 |
Dupilumab |
Dupixent® |
Dupilumab (Dupixent®) is indicated for the treatment of adults with moderate-to-severe prurigo nodularis who are candidates for systemic therapy. |
Rapid Review Complete |
24th August 2023 |
|
| 23044 |
Dupilumab |
Dupixent® |
Dupilumab (Dupixent®) is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (FeNO), who are inadequately controlled with medium to high dose inhaled corticosteroids (ICS) plus another medicinal product for maintenance treatment. |
Rapid Review Complete |
5th September 2023 |
|
| 21063 |
Dupilumab |
Dupixent® |
For adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (FeNO), who are inadequately controlled with high dose inhaled corticosteroids (ICS) plus another medicinal product for maintenance. |
Rapid review complete |
14th March 2024 |
|
| 21035 |
Dupilumab |
Dupixent® |
For severe atopic dermatitis in children 6 to 11 years old who are candidates for systemic therapy. |
Rapid review complete |
23rd September 2021 |
|
| 23042 |
Dupilumab |
Dupixent® |
Dupilumab is indicated for the treatment of severe atopic dermatitis in children aged 6 months to 6 years old who are candidates for systemic therapy. |
Rapid Review Complete |
1st September 2023 |
|
| 23046 |
Dupilumab |
Dupixent® |
Dupilumab (Dupixent®) is indicated as an add-on therapy with intranasal corticosteroids, for the treatment of adults with severe chronic rhinosinusitis with nasal polyposis for whom therapy with systemic corticosteroids and/or surgery do not provide adequate control. |
Rapid Review Complete |
5th September 2023 |
|
| - |
Dupilumab |
Dupixent® |
For treatment of moderate-to-severe atopic dermatitis in adult patients who are candidates for systemic therapy. |
NCPE Assessment Process Complete |
12th December 2019 |
|
| 24035 |
Dupilumab |
Dupixent® |
Dupilumab is indicated in adults as an add-on maintenance treatment for uncontrolled COPD characterised by raised blood eosinophils on a combination of an ICS, a LABA, and a LAMA, or on a combination of a LABA and a LAMA, if an ICS is not appropriate. |
Rapid Review Complete |
4th October 2024 |
|
| - |
Durvalumab |
Imfinzi® |
For the treatment of locally advanced, unresectable non-small cell lung cancer (NSCLC) in adults whose tumours express PD-L1 ≥1% on tumour cells and whose disease has not progressed following platinum-based chemo-radiation therapy (CRT). |
NCPE Assessment Process Complete |
7th May 2020 |
|
| 21033 |
Durvalumab |
Imfinzi® |
In combination with etoposide and either carboplatin or cisplatin, for the first-line treatment of adult patients with extensive-stage small cell lung cancer. |
Rapid review complete |
9th September 2021 |
|
| 23009 |
Durvalumab |
Imfinzi® |
Durvalumab in combination with gemcitabine and cisplatin is indicated for the first-line treatment of adults with unresectable or metastatic biliary tract cancer. |
NCPE assessment ongoing |
10th September 2024 |
|
| - |
Eculizumab |
Soliris® |
For the treatment of paroxysmal nocturnal haemoglobinuria (PNH) in the Irish healthcare setting. |
Assessment process complete |
14th October 2013 |
|
