Treatment Watch

2715 eventsUpdated today

FDA drug approvals, PDUFA decisions, orphan designations, and breakthrough therapy designations for rare diseases — sourced daily from FDA.gov.

FDA data is sourced from FDA.gov and openFDA.
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51 events · FDA approval · 2024

Dec 26
2024
FDA approvalOrphan drug
Tevimbra (tislelizumab-jsgr)

in combination with platinum and fluoropyrimidine-based chemotherapy, for the first-line treatment of adults with unresectable or metastatic HER2-negative gastric or gastroesophageal junction adenocarcinoma (G/GEJ) whose tumors express PD-L1 (greater than or equal to 1)

Adenocarcinoma of the oesophagus and oesophagogastric junction· BeOne Medicines USA, Inc.
Dec 20
2024
FDA approval
ALYFTREK (VANZACAFTOR, TEZACAFTOR, AND DEUTIVACAFTOR)FDA label ↗
· Vertex Pharmaceuticals Incorporated· NDA218730
Dec 19
2024
FDA approvalOrphan drug
Tryngolza (olezarsen)

adjunct to diet to reduce triglycerides in adults with familial chylomicronemia syndrome (FCS)

Familial chylomicronemia syndrome· Ionis Pharmaceuticals
Dec 18
2024
FDA approvalOrphan drug
Ryoncil (remestemcel-L-rknd)

treatment of steroid refractory acute graft versus host disease (SR-aGvHD) in pediatric patients 2 months of age and older

Acute graft versus host disease· Mesoblast, Inc.
Dec 13
2024
FDA approvalOrphan drug
Crenessity (crinecerfont)

adjunctive treatment to glucocorticoid replacement to control androgens in adults and pediatric patients 4 years of age and older with classic congenital adrenal hyperplasia (CAH)

Congenital adrenal hyperplasia· Neurocrine Biosciences, Inc.
Nov 22
2024
FDA approvalOrphan drug
Attruby (ACORAMIDIS HYDROCHLORIDE)

treatment of the cardiomyopathy of wild-type or variant transthyretin-mediated amyloidosis (ATTR-CM) in adults to reduce cardiovascular death and cardiovascular-related hospitalization

Hereditary transthyretin-mediated amyloidosis· BridgeBio Pharma, Inc.
Nov 13
2024
FDA approvalOrphan drug
Kebilidi (eladocagene exuparvovec-tneq)

treatment of adult and pediatric patients with aromatic L-amino acid decarboxylase (AADC) deficiency

Aromatic L-amino acid decarboxylase deficiency· PTC Therapeutics, Inc.
Nov 8
2024
FDA approvalOrphan drug
Aucatzyl (obecabtagene autoleucel)

treatment of adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL)

Acute lymphoblastic leukemia· Autolus Incorporated, US subsidiary of Autolus Limited
Nov 7
2024
FDA approval
DANZITEN (NILOTINIB)FDA label ↗
Chronic myeloid leukemia· Azurity Pharmaceuticals, Inc.· NDA219293
Nov 7
2024
FDA approvalOrphan drug
Danziten (nilotinib)

treatment of adult patients with newly diagnosed Philadelphia chromosome positive chronic myeloid leukemia (Ph+ CML) in chronic phase; and treatment of adult patients with chronic phase and accelerated phase Philadelphia chromosome positive chronic myelogenous leukemia (Ph+ CML) resistant or intolerant to prior therapy that included imatinib

Chronic myeloid leukemia· Azurity Pharmaceuticals, Inc.
Oct 16
2024
FDA approvalOrphan drug
Lumryz (sodium oxybate)

treatment of cataplexy or excessive daytime sleepiness (EDS) in patients 7 years of age and older with narcolepsy

Narcolepsy· Flamel Ireland Limited dba Avadel Ireland
Oct 11
2024
FDA approvalOrphan drug
HYMPAVZI (MARSTACIMAB-HNCQ)

routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adult and pediatric patients 12 years of age and older with hemophilia A (congenital factor VIII deficiency) without factor VIII inhibitors, or hemophilia B (congenital factor IX deficiency) without factor IX inhibitors

Czeizel-Losonci syndrome· Pfizer Laboratories Div Pfizer Inc
Sep 26
2024
FDA approval
MYCOPHENOLATE MOFETIL (MYCOPHENOLATE MOFETIL)
Mycophenolate mofetil embryopathy· Aurobindo Pharma Limited· ANDA218227
Sep 17
2024
FDA approvalOrphan drug
Fasenra (benralizumab)

treatment of adult patients with eosinophilic granulomatosis with polyangiitis (EGPA)

Eosinophilic granulomatosis with polyangiitis· AstraZeneca Pharmaceuticals LP
Sep 13
2024
FDA approval
PROCHLORPERAZINE EDISYLATE (PROCHLORPERAZINE EDISYLATE)
· Somerset Therapeutics, LLC· ANDA212257
Sep 5
2024
FDA approvalOrphan drug
Filspari (sparsentan)

to slow kidney function decline in adults with primary immunoglobulin A nephropathy (IgAN) who are at risk for disease progression

Immunoglobulin A nephropathy· Travere Therapeutics
Aug 30
2024
FDA approvalOrphan drug
PREVYMIS (letermovir)

prophylaxis of cytomegalovirus (CMV) infection and disease in adult and pediatric patients 6 months of age and older and weighing at least 6 kg who are CMV-seropositive recipients [R+] of an allogeneic hematopoietic stem cell transplant (HSCT)

Recurrent hepatitis C virus induced liver disease in liver transplant recipients· Merck Sharp & Dohme LLC
Aug 14
2024
FDA approvalOrphan drug
Livdelzi (seladelpar)

treatment of primary biliary cholangitis (PBC) in combination with ursodeoxycholic acid (UDCA) in adults who have had an inadequate response to UDCA, or as monotherapy in patients unable to tolerate UDCA

Primary biliary cholangitis· Gilead Sciences, Inc.
Aug 14
2024
FDA approvalOrphan drug
Niktimvo (axatilimab-csfr)

treatment of chronic graft-versus-host disease (cGVHD) after failure of at least two prior lines of systemic therapy in adult and pediatric patients weighing at least 40 kg

Chronic graft versus host disease· Incyte Corporation
Aug 9
2024
FDA approvalOrphan drug
Yorvipath (palopegteriparatide)

treatment of hypoparathyroidism in adults

Rare hypoparathyroidism· Ascendis Pharma Bone Diseases A/S
Aug 9
2024
FDA approval
NEFFY (EPINEPHRINE)FDA label ↗
X-linked immune dysregulation with inflammatory bowel disease due to ELF4 deficiency· ARS Pharmaceuticals Operations, Inc.· NDA214697
Aug 7
2024
FDA approvalOrphan drug
FABHALTA (IPTACOPAN)FDA label ↗
Immunoglobulin A nephropathy· Novartis Pharmaceuticals Corporation· NDA216064
Aug 7
2024
FDA approvalOrphan drug
Lymphir (denileukin diftitox-cxdl)

treatment of adult patients with relapsed or refractory Stage I-III cutaneous T-cell lymphoma (CTCL) after at least one prior systemic therapy

Primary cutaneous T-cell lymphoma· Citius Oncology, Inc.
Aug 6
2024
FDA approvalOrphan drug
Voranigo (vorasidenib)

treatment of adult and pediatric patients 12 years and older with Grade 2 astrocytoma or oligodendroglioma with a susceptible isocitrate dehydrogenase-1 (IDH1) or isocitrate dehydrogenase-2 (IDH2) mutation following surgery including biopsy, sub-total resection, or gross total resection

Angiocentric glioma· Servier Pharmaceuticals LLC
Aug 1
2024
FDA approvalOrphan drug
Tecelra (afamitresgene autoleucel)

treatment of adults with unresectable or metastatic synovial sarcoma who have received prior chemotherapy, are HLA-A*02:01P, -A*02:02P, -A02:03P, or -A*02:06P positive and whose tumor expresses the melanoma-associated antigen A4 (MAGE-A4) antigen as determined by FDA-approved or cleared companion diagnostic devices

Alveolar soft tissue sarcoma· USWM CT, LLC
Jul 24
2024
FDA approvalOrphan drug
Livmarli (MARALIXIBAT CHLORIDE)FDA label ↗

treatment of cholestatic pruritus in patients 12 months of age and older with progressive familial intrahepatic cholestasis (PFIC)

Progressive familial intrahepatic cholestasis· Mirum Pharmaceuticals Inc.· NDA214662
Jun 21
2024
FDA approvalOrphan drug
WAKIX (Pitolisant)

treatment of excessive daytime sleepiness (EDS) or cataplexy in adult patients with narcolepsy and treatment of EDS in pediatric patients 6 years of age and older with narcolepsy

Narcolepsy· Harmony Biosciences Management, Inc.
Jun 21
2024
FDA approvalOrphan drug
Vyvgart Hytrulo (EFGARTIGIMOD ALFA AND HYALURONIDASE (HUMAN RECOMBINANT))FDA label ↗

treatment of adult patients with chronic inflammatory demyelinating polyneuropathy (CIDP)

Chronic inflammatory demyelinating polyneuropathy· argenx US· BLA761304
Jun 14
2024
FDA approvalOrphan drug
Blincyto (blinatumomab)

treatment of CD19-positive Philadelphia chromosome-negative B-cell precursor acute lymphoblastic leukemia (ALL) in the consolidation phase of multiphase chemotherapy in adult and pediatric patients one month and older

Acute lymphoblastic leukemia· Amgen, Inc.
Jun 13
2024
FDA approval
TOPIRAMATE (TOPIRAMATE)
Lennox-Gastaut syndrome· Ascend Laboratories, LLC· ANDA218482
Jun 10
2024
FDA approvalOrphan drug
Iqirvo (elafibranor)

treatment of primary biliary cholangitis (PBC) in combination with ursodeoxycholic acid (UDCA) in adults who have had an inadequate response to UDCA, or as monotherapy in patients unable to tolerate UDCA

Primary biliary cholangitis· Ipsen Bioscience Inc.
Jun 6
2024
FDA approval
RYTELO (IMETELSTAT SODIUM)FDA label ↗
Myelodysplastic syndrome· Geron Corporation· NDA217779
May 30
2024
FDA approvalOrphan drug
Breyanzi (lisocabtagene maraleucel)

treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL) who have received at least 2 prior lines of systemic therapy, including a Bruton tyrosine kinase (BTK) inhibitor

Mantle cell lymphoma· Juno Therapeutics, Inc.
May 29
2024
FDA approvalOrphan drug
RETEVMO (selpercatinib)

treatment of adult and pediatric patients 2 years of age and older with advanced or metastatic medullary thyroid cancer (MTC) with a RET mutation, as detected by an FDA-approved test, who require systemic therapy; and treatment of adult and pediatric patients 2 years of age and older with advanced or metastatic thyroid cancer with a RET gene fusion, as detected by an FDA-approved test, who require systemic therapy and who are radioactive iodine-refractory (if radioactive iodine is appropriate)

Non-functioning neuroendocrine tumor of pancreas· Loxo Oncology Inc., a wholly owned subsidiary of Eli Lilly and Company
May 16
2024
FDA approvalOrphan drug
Imdelltra (tarlatamab-dlle)

treatment of adult patients with extensive stage small cell lung cancer (ES-SCLC) with disease progression on or after platinum-based chemotherapy

Small cell lung cancer· Amgen Inc.
Apr 26
2024
FDA approvalOrphan drug
Xolremdi (mavorixafor)

to increase the number of circulating mature neutrophils and lymphocytes in patients 12 years of age and older with WHIM syndrome (warts, hypogammaglobulinemia, infections and myelokathexis)

WHIM syndrome· X4 Pharmaceuticals, Inc.
Apr 25
2024
FDA approvalOrphan drug
Beqvez (fidanacogene elaparvovec-dzkt)

treatment of adults with moderate to severe hemophilia B (congenital factor IX deficiency) who: Currently use factor IX prophylaxis therapy, or; Have current or historical life-threatening hemorrhage, or; Have repeated, serious spontaneous bleeding episodes, and; Do not have neutralizing antibodies to adeno-associated virus serotype Rh74var (AAVRh74var) capsid as detected by an FDA-approved test

Moderate hemophilia B· Pfizer Inc.
Apr 24
2024
FDA approvalOrphan drug
Vijoice (alpelisib)

treatment of adult and pediatric patients 2 years of age and older with severe manifestations of PIK3CA-Related Overgrowth Spectrum (PROS) who require systemic therapy

PIK3CA-related overgrowth syndrome· Novartis Pharmaceuticals Corporation
Apr 23
2024
FDA approvalOrphan drug
Lutathera (lutetium Lu 177 dotatate)

treatment of adult and pediatric patients 12 years and older with somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (GEP-NETs), including foregut, midgut, and hindgut neuroendocrine tumors

Gastroenteropancreatic neuroendocrine neoplasm· Advanced Accelerator Applications
Apr 4
2024
FDA approvalOrphan drug
Abecma (idecabtagene vicleucel)

treatment of adult patients with relapsed or refractory multiple myeloma after two or more prior lines of therapy including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 monoclonal antibody

Multiple myeloma· Celgene Corporation, a Bristol-Myers Squibb Company
Mar 27
2024
FDA approval
VAFSEO (VADADUSTAT)FDA label ↗
· Akebia Therapeutics, Inc.· NDA215192
Mar 22
2024
FDA approvalOrphan drug
Opsynvi (MACITENTAN AND TADALAFIL)FDA label ↗

chronic treatment of adults with pulmonary arterial hypertension (PAH, WHO Group I and WHO Functional Class (FC) II-III)

Pulmonary arterial hypertension· Actelion Pharmaceuticals US, Inc.· NDA218490
Mar 21
2024
FDA approvalOrphan drug
DUVYZAT (GIVINOSTAT)

treatment of Duchenne muscular dystrophy (DMD) in patients 6 years of age and older

Duchenne and Becker muscular dystrophy· Italfarmaco SPA
Mar 19
2024
FDA approvalOrphan drug
Iclusig (ponatinib)

treatment of adult patients with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) in combination with chemotherapy

Precursor T-cell acute lymphoblastic leukemia· Takeda Pharmaceuticals U.S.A., Inc.
Mar 18
2024
FDA approvalOrphan drug
Spevigo (spesolimab-sbzo)

treatment of generalized pustular psoriasis (GPP) in adults and pediatric patients 12 years of age and older and weighing at least 40 kg

Generalized pustular psoriasis· Boehringer Ingelheim Pharmaceuticals, Inc. (BI)
Mar 18
2024
FDA approvalOrphan drug
Lenmeldy (ATIDARSAGENE AUTOTEMCEL)

treatment of children with pre-symptomatic late infantile (PSLI), pre-symptomatic early juvenile (PSEJ) or early symptomatic early juvenile (ESEJ) metachromatic leukodystrophy (MLD)

Metachromatic leukodystrophy, late infantile form· Orchard Therapeutics (Europe) Ltd· BLA125758
Mar 6
2024
FDA approvalOrphan drug
Besponsa (inotuzumab ozogamicin)

treatment of relapsed or refractory CD22-positive B-cell precursor acute lymphoblastic leukemia (ALL) in adult and pediatric patients 1 year and older

Precursor B-cell acute lymphoblastic leukemia· Wyeth Pharmaceuticals, LLC
Feb 28
2024
FDA approval
FINGOLIMOD (FINGOLIMOD)FDA label ↗
· Aurobindo Pharma Limited· ANDA207983
Feb 16
2024
FDA approvalOrphan drug
Amtagvi (lifileucel)

treatment of adult patients with unresectable or metastatic melanoma previously treated with a PD-1 blocking antibody, and if BRAF V600 mutation positive, a BRAF inhibitor with or without a MEK inhibitor

Primary melanoma of the central nervous system· Iovance Biotherapeutics, Inc.
Feb 9
2024
FDA approvalOrphan drug
Eohilia (budesonide)

treatment for 12 weeks in adult and pediatric patients 11 years of age and older with eosinophilic esophagitis (EoE)

Eosinophilic esophagitis· Takeda Pharmaceuticals U.S.A., Inc.
Jan 12
2024
FDA approvalOrphan drug
HyQvia (Immune Globulin Infusion 10% (Human) with Recombinant Human Hyaluronidase)

treatment of chronic inflammatory demyelinating polyneuropathy (CIDP) as maintenance therapy to prevent relapse of neuromuscular disability and impairment in adults

Chronic inflammatory demyelinating polyneuropathy· Takeda Development Center Americas, Inc.

Not medical advice — always consult your healthcare provider before making treatment decisions.

Data sourced from FDA.gov and openFDA, updated daily. Dates are subject to change. Always verify with FDA.gov for official decisions.