MFSD11

gene
On this page

Also known as FLJ22196FLJ20226

Summary

MFSD11 (major facilitator superfamily domain containing 11, HGNC:25458) is a protein-coding gene on chromosome 17q25.1, encoding UNC93-like protein MFSD11 (O43934).

Predicted to be located in membrane.

Source: NCBI Gene 79157 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 101 total — 2 pathogenic, 1 likely-pathogenic
  • MANE Select transcript: NM_001242532

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25458
Approved symbolMFSD11
Namemajor facilitator superfamily domain containing 11
Location17q25.1
Locus typegene with protein product
StatusApproved
AliasesFLJ22196, FLJ20226
Ensembl geneENSG00000092931
Ensembl biotypeprotein_coding
OMIM620346
Entrez79157

Gene structure

Transcript identifiers

Ensembl transcripts: 35 — 27 protein_coding, 4 nonsense_mediated_decay, 2 retained_intron, 2 protein_coding_CDS_not_defined

ENST00000336509, ENST00000355954, ENST00000585584, ENST00000585692, ENST00000585865, ENST00000585958, ENST00000586622, ENST00000586689, ENST00000588031, ENST00000588460, ENST00000588647, ENST00000588670, ENST00000588768, ENST00000590070, ENST00000590393, ENST00000590514, ENST00000591864, ENST00000593181, ENST00000621483, ENST00000685175, ENST00000869882, ENST00000869883, ENST00000869884, ENST00000869885, ENST00000869886, ENST00000869887, ENST00000869888, ENST00000869889, ENST00000869890, ENST00000936724, ENST00000936725, ENST00000970443, ENST00000970444, ENST00000970445, ENST00000970446

RefSeq mRNA: 10 — MANE Select: NM_001242532 NM_001242532, NM_001242533, NM_001242534, NM_001242535, NM_001242536, NM_001242537, NM_001353017, NM_001353018, NM_001353019, NM_024311

CCDS: CCDS11750, CCDS56045

Canonical transcript exons

ENST00000685175 — 13 exons

ExonStartEnd
ENSE000003354707673893876738993
ENSE000011935137674095776741064
ENSE000027989947673811976738448
ENSE000035386607675404776754087
ENSE000035747237674339876743456
ENSE000035881967674432276744466
ENSE000036143037676738676767451
ENSE000036335307676974676769871
ENSE000036354837677499776775171
ENSE000036554647674217776742273
ENSE000036638387677640676776541
ENSE000037866807674196976742048
ENSE000039323507677818876779341

Expression profiles

Bgee: expression breadth ubiquitous, 244 present calls, max score 93.31.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 25.2459 / max 234.0484, expressed in 1818 samples.

FANTOM5 promoters (9 alternative TSS)

Promoter IDTPM avgSamples expressed
1629037.75591758
1629027.62891748
1629043.03481192
1628992.67111441
1628981.8548951
1629061.6045492
2083830.5325268
1629000.119027
1629010.04448

Top tissues by expression

252 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
buccal mucosa cellCL:000233693.31gold quality
adrenal tissueUBERON:001830390.57gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099190.13gold quality
ileal mucosaUBERON:000033189.89gold quality
bone marrow cellCL:000209289.68gold quality
rectumUBERON:000105289.28gold quality
spermCL:000001989.23gold quality
apex of heartUBERON:000209889.15gold quality
left testisUBERON:000453389.05gold quality
lower esophagus mucosaUBERON:003583489.05gold quality
islet of LangerhansUBERON:000000689.01gold quality
right testisUBERON:000453488.96gold quality
muscle of legUBERON:000138388.94gold quality
right atrium auricular regionUBERON:000663188.87gold quality
gastrocnemiusUBERON:000138888.71gold quality
left ventricle myocardiumUBERON:000656688.66gold quality
monocyteCL:000057688.62gold quality
cardiac atriumUBERON:000208188.45gold quality
leukocyteCL:000073888.44gold quality
hindlimb stylopod muscleUBERON:000425288.22gold quality
vaginaUBERON:000099688.18gold quality
skin of abdomenUBERON:000141687.85gold quality
cardiac muscle of right atriumUBERON:000337987.82gold quality
skin of legUBERON:000151187.78gold quality
tibialis anteriorUBERON:000138587.75gold quality
adenohypophysisUBERON:000219687.71gold quality
testisUBERON:000047387.69gold quality
smooth muscle tissueUBERON:000113587.57gold quality
esophagus mucosaUBERON:000246987.47gold quality
mucosa of transverse colonUBERON:000499187.45gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 2.

ExperimentMarker?Max mean expression
E-CURD-112yes13.98
E-ANND-3yes8.22

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

39 targeting MFSD11, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-4425100.0067.591049
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-126-5P100.0072.713180
HSA-MIR-4789-3P99.9970.752484
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-368699.9070.532432
HSA-MIR-990299.8969.152250
HSA-MIR-7162-3P99.8968.161682
HSA-MIR-1211999.8768.351653
HSA-MIR-4799-5P99.8270.602663
HSA-MIR-62399.7668.161170
HSA-MIR-132-3P99.7370.561424
HSA-MIR-212-3P99.7370.651424
HSA-MIR-4755-5P99.7170.342716
HSA-MIR-5006-3P99.7170.262728
HSA-MIR-58799.6470.862611
HSA-MIR-94099.3766.142064
HSA-MIR-6808-5P99.3166.232150
HSA-MIR-6893-5P99.3166.252119
HSA-MIR-504-3P99.3067.181745
HSA-MIR-3064-5P99.2666.131497
HSA-MIR-3085-3P99.2666.161490
HSA-MIR-6504-5P99.2665.951487
HSA-MIR-6504-3P99.1769.312891
HSA-MIR-10399-5P99.1769.872610
HSA-MIR-125399.1267.081688
HSA-MIR-7151-3P99.0469.722370
HSA-MIR-4724-5P98.8767.751324
HSA-MIR-942-3P98.8169.04876
HSA-MIR-465698.7966.221306

Literature-anchored findings (GeneRIF, showing 1)

  • Results from a study on gene expression variability markers in early-stage human embryos shows that MFSD11 is a putative marker for the 3-day, 8-cell embryo stage. (PMID:26288249)

Cross-species orthologs

21 orthologs

OrganismSymbolGene ID
danio_reriomfsd11ENSDARG00000102828
mus_musculusMfsd11ENSMUSG00000020818
rattus_norvegicusMfsd11ENSRNOG00000000247
drosophila_melanogasterCG18549FBGN0038053
caenorhabditis_elegansWBGENE00007774
caenorhabditis_elegansWBGENE00009485
caenorhabditis_elegansWBGENE00010925
caenorhabditis_elegansWBGENE00012428
caenorhabditis_elegansWBGENE00012535
caenorhabditis_elegansWBGENE00012686
caenorhabditis_elegansWBGENE00012688
caenorhabditis_elegansWBGENE00015258
caenorhabditis_elegansWBGENE00015260
caenorhabditis_elegansWBGENE00015592
caenorhabditis_elegansWBGENE00017944
caenorhabditis_elegansWBGENE00017945
caenorhabditis_elegansWBGENE00021448
caenorhabditis_elegansWBGENE00021797
caenorhabditis_elegansWBGENE00021798
caenorhabditis_elegansWBGENE00022641
caenorhabditis_elegansWBGENE00022643

Protein

Protein identifiers

UNC93-like protein MFSD11O43934 (reviewed: O43934)

Alternative names: Major facilitator superfamily domain-containing protein 11, Protein ET

All UniProt accessions (8): O43934, K7ELU3, K7EM95, K7EMP0, K7EQL2, K7ERE5, K7ES57, K7ES99

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Similarity. Belongs to the unc-93 family.

Isoforms (2)

UniProt IDNamesCanonical?
O43934-11yes
O43934-22

RefSeq proteins (10): NP_001229461, NP_001229462, NP_001229463, NP_001229464, NP_001229465, NP_001229466, NP_001339946, NP_001339947, NP_001339948, NP_077287 (=MANE)

Domains & families (InterPro)

IDNameType
IPR010291Ion_channel_UNC-93Family
IPR036259MFS_trans_sfHomologous_superfamily
IPR051617UNC-93-like_regulatorFamily

Pfam: PF05978

UniProt features (18 total): transmembrane region 12, sequence variant 2, chain 1, modified residue 1, glycosylation site 1, splice variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-O43934-F187.720.62

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (1): 204

Glycosylation sites (1): 40

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 114 (showing top): GSE45365_CTRL_VS_MCMV_INFECTION_NK_CELL_UP, GOBP_RESPONSE_TO_FOOD, MILI_PSEUDOPODIA_CHEMOTAXIS_DN, GOBP_RESPONSE_TO_STARVATION, MARSON_BOUND_BY_FOXP3_STIMULATED, MARSON_BOUND_BY_FOXP3_UNSTIMULATED, ARNT2_TARGET_GENES, BARX1_TARGET_GENES, CHAF1B_TARGET_GENES, CIITA_TARGET_GENES, CREB3L4_TARGET_GENES, EMX1_TARGET_GENES, FOXE1_TARGET_GENES, GTF2E2_TARGET_GENES, HHEX_TARGET_GENES

GO Biological Process (2): response to food (GO:0032094), response to starvation (GO:0042594)

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (1): membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
response to nutrient levels2
response to chemical1
response to stress1
binding1
cellular anatomical structure1

Protein interactions and networks

STRING

1010 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
MFSD11SLC61A1Q6N075771
MFSD11SLC67A2Q8NBP5670
MFSD11MFSD6LQ8IWD5651
MFSD11SLC33A2Q96ES6645
MFSD11SLC68A1Q14CX5642
MFSD11SVOPLQ8N434640
MFSD11SLC75A1Q14728625
MFSD11MFSD12Q6NUT3624
MFSD11SVOPQ8N4V2620
MFSD11MFSD6Q6ZSS7607
MFSD11SPNS3Q6ZMD2548
MFSD11METTL23Q86XA0544
MFSD11MFSD8Q8NHS3540
MFSD11SPNS1Q9H2V7539
MFSD11SLC71A1Q96MC6539

IntAct

23 interactions, top by confidence:

ABTypeScore
MFSD11GJB3psi-mi:“MI:0915”(physical association)0.560
MFSD11GJA8psi-mi:“MI:0915”(physical association)0.560
MFSD11FXYD3psi-mi:“MI:0915”(physical association)0.560
MFSD11PIK3IP1psi-mi:“MI:0915”(physical association)0.560
MFSD11LAYNpsi-mi:“MI:0915”(physical association)0.560
MFSD11PVRpsi-mi:“MI:0915”(physical association)0.560
MFSD11UBE2Q1psi-mi:“MI:0914”(association)0.530
MFSD11AGPAT2psi-mi:“MI:0914”(association)0.350
MFSD11PLD2psi-mi:“MI:0914”(association)0.350
MFSD11FXYD3psi-mi:“MI:0915”(physical association)0.000
MFSD11PIK3IP1psi-mi:“MI:0915”(physical association)0.000
MFSD11LAYNpsi-mi:“MI:0915”(physical association)0.000
MFSD11PVRpsi-mi:“MI:0915”(physical association)0.000

BioGRID (43): MFSD11 (Two-hybrid), SMAP2 (Affinity Capture-MS), UBE2Q1 (Affinity Capture-MS), TUBB1 (Affinity Capture-MS), MFSD11 (Affinity Capture-RNA), MFSD11 (Affinity Capture-RNA), MFSD11 (Two-hybrid), MFSD11 (Two-hybrid), PIK3IP1 (Two-hybrid), GJA8 (Two-hybrid), GJB3 (Two-hybrid), LAYN (Two-hybrid), UBE2Q1 (Affinity Capture-MS), TUBB1 (Affinity Capture-MS), TMCO1 (Affinity Capture-MS)

ESM2 similar proteins: A6QQU6, A8MRY9, B3LFA3, B8AF63, F4JKQ7, O43934, O80605, P57057, P57758, Q03411, Q0D7E4, Q10R54, Q39231, Q39232, Q3TIT8, Q4R495, Q5F3N0, Q5M7K3, Q5RCQ5, Q5RD30, Q5RKH7, Q640L2, Q67YF8, Q6A329, Q6DIT7, Q6GPQ3, Q6P499, Q6PB15, Q6YK44, Q7Z5S9, Q8AVC3, Q8BGN5, Q8BJ51, Q8GWX2, Q8GYS1, Q8H4H5, Q8NCC5, Q8VE96, Q8VEH0, Q944N8

Diamond homologs: O43934, Q4R495, Q5RCQ5, Q6DIT7, Q6PB15, Q8BJ51

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

101 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic2
Likely pathogenic1
Uncertain significance69
Likely benign5
Benign1

Top pathogenic / likely-pathogenic (3)

Variant IDHGVSClassification
2504111NM_001195427.2(SRSF2):c.284C>T (p.Pro95Leu)Pathogenic
3765039NM_001195427.2(SRSF2):c.284C>A (p.Pro95His)Pathogenic
998075NM_001195427.2(SRSF2):c.284C>G (p.Pro95Arg)Likely pathogenic

SpliceAI

3116 predictions. Top by Δscore:

VariantEffectΔscore
17:76736180:T:TAdonor_gain1.0000
17:76740935:C:Aacceptor_gain1.0000
17:76740941:T:TAacceptor_gain1.0000
17:76740944:ATTAT:Aacceptor_gain1.0000
17:76740945:T:Gacceptor_gain1.0000
17:76740947:A:AGacceptor_gain1.0000
17:76740947:AT:Aacceptor_gain1.0000
17:76740948:T:Gacceptor_gain1.0000
17:76740948:T:TAacceptor_gain1.0000
17:76740955:A:AGacceptor_gain1.0000
17:76740955:AGCAT:Aacceptor_gain1.0000
17:76740956:G:GAacceptor_gain1.0000
17:76740956:GC:Gacceptor_gain1.0000
17:76740956:GCAT:Gacceptor_gain1.0000
17:76740956:GCATG:Gacceptor_gain1.0000
17:76741967:A:AGacceptor_gain1.0000
17:76741968:G:GGacceptor_gain1.0000
17:76741968:GC:Gacceptor_gain1.0000
17:76741968:GCAT:Gacceptor_gain1.0000
17:76742050:T:Adonor_loss1.0000
17:76742162:T:TAacceptor_gain1.0000
17:76742163:G:Aacceptor_gain1.0000
17:76742175:A:AGacceptor_gain1.0000
17:76742176:G:GGacceptor_gain1.0000
17:76742176:GT:Gacceptor_gain1.0000
17:76744317:C:CAacceptor_gain1.0000
17:76744319:TA:Tacceptor_loss1.0000
17:76744320:A:AGacceptor_gain1.0000
17:76744320:A:Cacceptor_loss1.0000
17:76744321:G:GGacceptor_gain1.0000

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000020615 (17:76793764 T>C), RS1000061451 (17:76793936 A>G), RS1000108320 (17:76745988 T>C,G), RS1000117888 (17:76739962 C>G), RS1000130835 (17:76758192 A>T), RS1000196998 (17:76786402 A>G), RS1000212375 (17:76774554 T>C), RS1000213558 (17:76799811 AG>A), RS1000229626 (17:76739708 C>T), RS1000300889 (17:76787004 G>A), RS1000311884 (17:76746311 G>A,C,T), RS1000338311 (17:76739870 C>G,T), RS1000369404 (17:76767522 A>G), RS1000409899 (17:76736096 C>G,T), RS1000447873 (17:76756604 T>C)

Disease associations

OMIM: gene MIM:620346 | disease phenotypes: MIM:601626

GenCC curated gene-disease

Mondo (3): atypical chronic myeloid leukemia, BCR-ABL1 negative (MONDO:0004653), acute myeloid leukemia (MONDO:0018874), acute megakaryoblastic leukemia in down syndrome (MONDO:0020526)

Orphanet (3): Acute myeloid leukemia (Orphanet:519), Atypical chronic myeloid leukemia (Orphanet:98824), Acute megakaryoblastic leukemia in children with Down syndrome (Orphanet:99887)

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

1 associations (top):

StudyTraitp-value
GCST002071_2Retinal arteriolar caliber2.000000e-10

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004731eye measurement

MeSH disease descriptors (1)

DescriptorNameTree numbers
D015470Leukemia, Myeloid, AcuteC04.557.337.539.275; C15.378.508.539.275

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

21 total (human), top 21 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidincreases expression3
sodium arsenitedecreases expression, increases abundance, increases expression, affects cotreatment2
FR900359increases phosphorylation1
bisphenol Faffects cotreatment, increases methylation1
triphenyl phosphateaffects expression1
beta-lapachoneincreases expression1
manganese chlorideaffects cotreatment, decreases expression, increases abundance1
K 7174increases expression1
ICG 001increases expression1
bisphenol Sdecreases methylation1
4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic acidincreases expression1
Fulvestrantaffects cotreatment, increases methylation1
Acetaminophenincreases expression1
Arsenicaffects cotreatment, decreases expression, increases abundance1
Manganeseaffects cotreatment, decreases expression, increases abundance1
Quercetinincreases expression1
Cyclosporineincreases expression1
Aflatoxin B1increases methylation1
Asbestos, Crocidolitedecreases expression1
Cadmium Chlorideincreases expression1
Acrylamideincreases expression1

Cellosaurus cell lines

2 cell lines: 2 cancer cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_D4G9HCT116-MFSD11-KO-c16Cancer cell lineMale
CVCL_D4GAHCT116-MFSD11-KO-c17Cancer cell lineMale

Clinical trials (associated diseases)

300 trials via MONDO — disease-level, not drug-specific.

TrialPhaseStatusTitle
NCT00199147PHASE4UNKNOWNEfficacy of G-CSF-Priming in Elderly AML Patients
NCT00304447PHASE4COMPLETEDStudy Evaluating the Effect of Corticosteroids on Mylotarg® Infusion-Related Adverse Events in Patients With Leukemia
NCT00464217PHASE4COMPLETEDTreatment of the Acute Myeloblastic Leukaemia in Patients Over 65 Years
NCT00487448PHASE4COMPLETEDSMD_FLAG-IDA_98: FLAG-IDA in Induction Treatment of High Risk Myelodysplastic Syndromes or Secondary Acute Myeloblastic Leukemia
NCT00488709PHASE4COMPLETEDFludarabine, Cytarabine, Topotecan in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia
NCT00686543PHASE4COMPLETEDOral Posaconazole in High Risk Patients With Gastrointestinal Dysfunction (Study P05115)
NCT01041040PHASE4COMPLETEDLAM07: Study to Analyze the Efficacy of a Risk Adapted Treatment Strategy, Including Gemtuzumab Ozogamicin (GO) During Consolidation, for Patients With Acute Myeloid Leukemia (AML)
NCT01198054PHASE4TERMINATEDLENA-LMA-5:Lenalidomide in Acute Myeloid Leukemia (AML)
NCT01200355PHASE4COMPLETEDPosaconazole Versus Micafungin for Prophylaxis Against Invasive Fungal Infections During Neutropenia in Patients Undergoing Chemotherapy for Acute Myelogenous Leukemia, Acute Lymphocytic Leukemia or Myelodysplastic Syndrome
NCT01347996PHASE4COMPLETEDMaintenance Therapy With Ceplene® (Histamine) and IL-2 on Immune Response and MRD in Acute Myeloid Leukemia
NCT01587430PHASE4UNKNOWN3 Anthracyclines, 2 Types of Consolidation With Different ARA-C Doses and Maintenance in Adult Acute Myeloid Leukemia
NCT01819792PHASE4COMPLETEDRespiratory Viral Infections During Acute Myeloid Leukemia (AML)Chemotherapy Related Aplasia
NCT02024308PHASE4UNKNOWNAML1-ETO Acute Myeloid Leukemia With Fludarabine and Cytarabine Chemotherapy
NCT02027064PHASE4UNKNOWNInterferon for the Intervention of Molecular Relapse in t (8; 21) AML After Allo-HSCT
NCT02277847PHASE4UNKNOWNIdarubicin at Different Dosages as Induction Therapy for Newly Diagnosed Acute Myeloid Leukaemia
NCT02386800PHASE4ACTIVE_NOT_RECRUITINGCINC424A2X01B Rollover Protocol
NCT02926586PHASE4COMPLETEDFludarabine and Cytarabine Versus High-dose Cytarabine for CBF-AML
NCT02933333PHASE4UNKNOWNG-CSF Alone or Combination With GM-CSF on Prevention and Treatment of Infection in Children With Malignant Tumor
NCT03026842PHASE4UNKNOWNDecitabine Versus Conventional Chemotherapy for Maintenance Therapy of Acute Myeloid Leukemia With t(8;21)
NCT03150134PHASE4UNKNOWNEarly Tapering of Immunosuppressive Agents to Immunomodulation to Improve Survival of AML Patients
NCT05144243PHASE4ACTIVE_NOT_RECRUITINGStudy to Assess Adverse Events and Change in Disease State of Oral Venetoclax in Combination With Subcutaneous (SC) Azacitidine in Newly Diagnosed Adult Participants With Acute Myeloid Leukemia (AML) Who Are Ineligible for Intensive Chemotherapy in China
NCT06370000PHASE4RECRUITINGOral Azacitidine in Transplant-Eligible Patients With Acute Myeloid Leukemia (AML) Suffering From Health-Inequality
NCT06571825PHASE4RECRUITINGRIC Allo-HSCT vs. Venetoclax-Based Consolidation in Elderly AML Patients After First CR
NCT07016165PHASE4RECRUITINGCiprofloxacin vs Ceftazidime for Empirical Treatment of High-Risk Neutropenic Fever in Children With Hematologic Malignancies
NCT07044687PHASE4RECRUITINGStudy to Assess Adverse Events and Change in Disease Activity of Oral Venetoclax in Combination With Subcutaneous (SC) or Intravenous (IV) Azacitidine in Newly Diagnosed Adult Participants With Acute Myeloid Leukemia (AML) Who Are Ineligible for Standard Induction Therapy in India
NCT07486713PHASE4RECRUITINGOlutasidenib DDI Study in Patients With IDH1 Mutation Positive Malignancies
NCT07561892PHASE4RECRUITINGStudy of the Effectiveness and Safety of Daunorubicin /Idarubicin ± Silibinin in Treating Newly Diagnosed AML (Non-M3).
NCT00000589PHASE3COMPLETEDTrial to Reduce Alloimmunization to Platelets (TRAP)
NCT00044486PHASE3COMPLETEDProphylaxis Trial of Posaconazole Versus Standard Azole Therapy for Neutropenic Patients (Study P01899)
NCT00093990PHASE3COMPLETEDTipifarnib Versus Best Supportive Care in the Treatment of Newly Diagnosed Acute Myeloid Leukemia (AML)
NCT00125606PHASE3TERMINATEDPhase 3 Trial for AML Patients in CR2 Comparing 8Gy TBI /Fludarabine to Conditioning With TBI 12Gy/Cyclophosphamide
NCT00136084PHASE3COMPLETEDTreatment of Patients With Newly Diagnosed Acute Myeloid Leukemia or Myelodysplasia
NCT00146120PHASE3COMPLETEDRisk-Adapted Therapy of Acute Myeloid Leukemia of Adults (18-60 Years) According to the Cytogenetic Result
NCT00150878PHASE3TERMINATEDStandard vs. Reduced-Intensity Conditioning in Patients With Acute Myeloid Leukemia in First Remission
NCT00151255PHASE3COMPLETEDAll-Trans Retinoic Acid in Combination With Standard Induction and Consolidation Therapy in Older Patients With Newly Diagnosed Acute Myeloid Leukemia
NCT00152139PHASE3COMPLETEDStem Cell Transplantation for Patients With Hematologic Malignancies
NCT00152594PHASE3TERMINATEDVoriconazole or Placebo in the Prophylaxis of Lung Infiltrates in Patients Undergoing Induction Chemotherapy for Acute Myelogenous Leukemia
NCT00186966PHASE3COMPLETEDTreatment of Children and Adolescents With Refractory or Relapsed Acute Myeloid Leukemia
NCT00226512PHASE3WITHDRAWNTo Determine the Role of Adding Campath-1H or ATG Given In-vivo in Addition to Fludarabine and Low Dose Busulfex on Outcome in Patients Treated With Reduced Intensity Conditioning
NCT00260832PHASE3COMPLETEDTrial of Decitabine in Patients With Acute Myeloid Leukemia