ACRBP

gene
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Also known as SP32OY-TES-1CT23

Summary

ACRBP (acrosin binding protein, HGNC:17195) is a protein-coding gene on chromosome 12p13.31, encoding Acrosin-binding protein (Q8NEB7). Acrosomal protein that maintains proacrosin (pro-ACR) as an enzymatically inactive zymogen in the acrosome.

The protein encoded by this gene is similar to proacrosin binding protein sp32 precursor found in mouse, guinea pig, and pig. This protein is located in the sperm acrosome and is thought to function as a binding protein to proacrosin for packaging and condensation of the acrosin zymogen in the acrosomal matrix. This protein is a member of the cancer/testis family of antigens and it is found to be immunogenic. In normal tissues, this mRNA is expressed only in testis, whereas it is detected in a range of different tumor types such as bladder, breast, lung, liver, and colon.

Source: NCBI Gene 84519 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 93 total — 4 pathogenic
  • MANE Select transcript: NM_032489

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:17195
Approved symbolACRBP
Nameacrosin binding protein
Location12p13.31
Locus typegene with protein product
StatusApproved
AliasesSP32, OY-TES-1, CT23
Ensembl geneENSG00000111644
Ensembl biotypeprotein_coding
OMIM608352
Entrez84519

Gene structure

Transcript identifiers

Ensembl transcripts: 9 — 4 protein_coding, 2 retained_intron, 2 protein_coding_CDS_not_defined, 1 nonsense_mediated_decay

ENST00000229243, ENST00000414226, ENST00000535884, ENST00000536350, ENST00000538524, ENST00000540513, ENST00000542357, ENST00000544352, ENST00000546114

RefSeq mRNA: 1 — MANE Select: NM_032489 NM_032489

CCDS: CCDS8554

Canonical transcript exons

ENST00000229243 — 10 exons

ExonStartEnd
ENSE0000071544366435396643671
ENSE0000071559466467946647012
ENSE0000086693466441376644605
ENSE0000231450066473246647432
ENSE0000352749166400606640227
ENSE0000352769766464836646577
ENSE0000357433766452206645337
ENSE0000357449166380756638404
ENSE0000364779966389546639037
ENSE0000366344966403436640522

Expression profiles

Bgee: expression breadth ubiquitous, 177 present calls, max score 99.16.

FANTOM5 (CAGE): breadth broad, TPM avg 6.1225 / max 1145.3048, expressed in 725 samples.

FANTOM5 promoters (7 alternative TSS)

Promoter IDTPM avgSamples expressed
1291522.8152608
1291441.8849118
1291451.1389116
1291530.184635
1291510.076114
2065540.01214
1291500.01083

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
left testisUBERON:000453399.16gold quality
right testisUBERON:000453498.89gold quality
monocyteCL:000057698.42gold quality
leukocyteCL:000073898.11gold quality
spermCL:000001997.40gold quality
adult organismUBERON:000702397.23gold quality
testisUBERON:000047396.85gold quality
granulocyteCL:000009495.03gold quality
bloodUBERON:000017892.32gold quality
spleenUBERON:000210689.96gold quality
right lungUBERON:000216788.14gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099187.16gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047387.13gold quality
corpus epididymisUBERON:000435985.25gold quality
bone marrow cellCL:000209282.61gold quality
bone marrowUBERON:000237180.17gold quality
right uterine tubeUBERON:000130279.91gold quality
left lobe of thyroid glandUBERON:000112079.80gold quality
right lobe of thyroid glandUBERON:000111979.69gold quality
upper lobe of left lungUBERON:000895279.56gold quality
thyroid glandUBERON:000204679.53gold quality
trabecular bone tissueUBERON:000248377.99gold quality
right hemisphere of cerebellumUBERON:001489077.97gold quality
cerebellar hemisphereUBERON:000224577.58gold quality
upper lobe of lungUBERON:000894877.49gold quality
cerebellar cortexUBERON:000212977.38gold quality
cerebellumUBERON:000203776.21gold quality
gall bladderUBERON:000211075.52gold quality
islet of LangerhansUBERON:000000675.49gold quality
vermiform appendixUBERON:000115475.35gold quality

Single-cell (SCXA)

Detected in 8 experiment(s), a significant marker in 8.

ExperimentMarker?Max mean expression
E-MTAB-10432yes5545.83
E-MTAB-9221yes4762.73
E-MTAB-7407yes3936.47
E-GEOD-150728yes3200.67
E-HCAD-4yes33.00
E-GEOD-134144yes29.34
E-HCAD-1yes9.22
E-ANND-3no0.00

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

21 targeting ACRBP, 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-10401-5P99.9965.79948
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-MIR-6721-5P99.9368.922981
HSA-MIR-4731-5P99.8967.232537
HSA-MIR-449299.8768.253611
HSA-MIR-449599.8272.083080
HSA-MIR-1212499.6869.172700
HSA-MIR-449899.4767.422360
HSA-MIR-128-1-5P99.3360.46332
HSA-MIR-128-2-5P99.3360.83311
HSA-MIR-3925-5P99.2167.901466
HSA-MIR-6814-5P99.0366.681273
HSA-MIR-330-5P98.7367.631788
HSA-MIR-32698.2566.441565
HSA-MIR-473697.9665.891287
HSA-MIR-3620-5P97.4263.95792
HSA-MIR-158796.9564.03932
HSA-MIR-429696.3563.551233
HSA-MIR-6747-5P96.1764.99743

Literature-anchored findings (GeneRIF, showing 9)

  • We showed identification of HLA-A24-binding OY-TES-1 peptide, TES(401-409) (KTPFVSPLL) recognized by CD8 T-cells. (PMID:16301813)
  • High ACRBP expression correlated with reduced survival time and faster relapse among ovarian cancer patients. (PMID:20876808)
  • The down-regulation of OY-TES-1 expression in bone marrow-derived mesenchymal stem cells caused cell growth inhibition, cell cycle arrest, apoptosis induction and migration ability attenuation. (PMID:22651134)
  • OY-TES-1 is frequently expressed in colorectal carcinoma and is able to induce humoral immune response spontaneously in CRC patients. (PMID:24294369)
  • OY-TES-1 downregulation in liver cancer cells caused 2 opposite effects on cell proliferation: promotion by upregulating CCND2 and CDCA3, and inhibition by CD9 upregulation and NANOG downregulation. OY-TES-1 may play multiple roles in liver cancer. (PMID:25673160)
  • OY-TES-1 was expressed in ovarian cancer (OC) tissues with a high proportion, and some of OC tissues presented OY-TES-1 expression in high level vs OC adjacent tissues. (PMID:26189257)
  • Down regulation of OY-TES-1 increased expression of apoptosis-regulated protein caspase-3, and decreased expression of cell cycle-regulated protein cyclin E, migration/invasion-regulated proteins MMP2 and MMP9. (PMID:26339343)
  • Cancer-testis Antigen OY-TES-1 Expression and Immunogenicity in Hepatocellular Carcinoma. (PMID:32862383)
  • CT23 knockdown attenuating malignant behaviors of hepatocellular carcinoma cell is associated with upregulation of metallothionein 1. (PMID:33559934)

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusAcrbpENSMUSG00000072770
rattus_norvegicusAcrbpENSRNOG00000017399

Protein

Protein identifiers

Acrosin-binding proteinQ8NEB7 (reviewed: Q8NEB7)

Alternative names: Acrosin-binding protein, 60 kDa form, Cancer/testis antigen 23, Cancer/testis antigen OY-TES-1, Proacrosin-binding protein sp32

All UniProt accessions (6): Q8NEB7, A0A140VJD6, E7EP66, F5H2C2, F5H3P4, F5H5S8

UniProt curated annotations — full annotation on UniProt →

Function. Acrosomal protein that maintains proacrosin (pro-ACR) as an enzymatically inactive zymogen in the acrosome. Involved also in the acrosome formation.

Subunit / interactions. Binds proacrosin (pro-ACR). Does not bind the mature form of ACR.

Subcellular location. Secreted. Cytoplasmic vesicle. Secretory vesicle. Acrosome.

Tissue specificity. Expression restricted to testis in normal tissue. Expressed in a wide spectrum of cancers, including bladder, breast, liver, lung and colon cancers.

Post-translational modifications. Phosphorylated on Tyr residues in capacitated sperm. The N-terminus is blocked. Synthesized as a 60-kDa precursor, the 32-kDa mature form is post-translationally produced by the removal of the N-terminal half of the precursor during sperm maturation in the testis and/or epididymis.

RefSeq proteins (1): NP_115878* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR009865Proacrosin-bdFamily
IPR036058Kazal_dom_sfHomologous_superfamily

Pfam: PF07222

UniProt features (13 total): region of interest 3, compositionally biased region 3, chain 2, sequence conflict 2, signal peptide 1, sequence variant 1, propeptide 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NEB7-F164.090.25

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 94 (showing top): WHITEHURST_PACLITAXEL_SENSITIVITY, GOCC_SECRETORY_GRANULE, GOBP_VESICLE_ORGANIZATION, KORKOLA_CHORIOCARCINOMA_DN, GOBP_MALE_GAMETE_GENERATION, GOBP_SECRETORY_GRANULE_ORGANIZATION, GOBP_CELLULAR_COMPONENT_ASSEMBLY_INVOLVED_IN_MORPHOGENESIS, KORKOLA_EMBRYONAL_CARCINOMA_DN, GOBP_ACROSOME_ASSEMBLY, GOBP_ORGANELLE_ASSEMBLY, GOBP_CELLULAR_PROCESS_INVOLVED_IN_REPRODUCTION_IN_MULTICELLULAR_ORGANISM, GOBP_ENDOMEMBRANE_SYSTEM_ORGANIZATION, GOBP_DEVELOPMENTAL_PROCESS_INVOLVED_IN_REPRODUCTION, CCCAGAG_MIR326, GOBP_FERTILIZATION

GO Biological Process (3): acrosome assembly (GO:0001675), spermatid development (GO:0007286), fertilization (GO:0009566)

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

GO Cellular Component (5): acrosomal vesicle (GO:0001669), acrosomal membrane (GO:0002080), extracellular region (GO:0005576), nucleus (GO:0005634), cytoplasmic vesicle (GO:0031410)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
developmental process involved in reproduction1
spermatid development1
cellular component assembly involved in morphogenesis1
cellular process involved in reproduction in multicellular organism1
secretory granule organization1
organelle assembly1
germ cell development1
spermatid differentiation1
sexual reproduction1
reproductive process1
binding1
secretory granule1
acrosomal vesicle1
secretory granule membrane1
cellular anatomical structure1
intracellular membrane-bounded organelle1
cytoplasm1
intracellular vesicle1

Protein interactions and networks

STRING

1004 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ACRBPLIPIQ6XZB0690
ACRBPZPBP2Q6X784686
ACRBPACRP10323654
ACRBPZPBPQ9BS86649
ACRBPSPA17Q15506646
ACRBPADAM2P78326618
ACRBPCAGE1Q8TC20606
ACRBPSAGE1Q9NXZ1595
ACRBPPRSS50Q9UI38580
ACRBPSPACA3Q8IXA5561
ACRBPMAGEC1O60732540
ACRBPSPACA1Q9HBV2537
ACRBPSPAM1P38567522
ACRBPAKAP3O75969518
ACRBPODF1Q14990500

IntAct

4 interactions, top by confidence:

ABTypeScore
ACRBPMYO9Apsi-mi:“MI:0914”(association)0.350
MAN2B1IGF2Rpsi-mi:“MI:0914”(association)0.350
ACRBPSBNO1psi-mi:“MI:0914”(association)0.350

BioGRID (21): ACRBP (Affinity Capture-MS), ACRBP (Positive Genetic), MYO5C (Affinity Capture-MS), ARFGAP2 (Affinity Capture-MS), MBD3 (Affinity Capture-MS), CEP164 (Affinity Capture-MS), MYO9A (Affinity Capture-MS), TOR3A (Affinity Capture-MS), DEPDC1B (Affinity Capture-MS), ACRBP (Affinity Capture-MS), ACRBP (Affinity Capture-MS), PTOV1 (Affinity Capture-MS), MTA3 (Affinity Capture-MS), IQGAP3 (Affinity Capture-MS), RIPK4 (Affinity Capture-MS)

ESM2 similar proteins: A2A699, A2ALI5, A2AWH2, A2BD09, A2BDP1, A4IFM1, A4IHZ3, A6QLD2, A6QPA0, A8MVW0, B0BN44, B1AL88, F1N4E5, O14525, O15105, O35144, O35253, O75129, O75949, O88406, O94983, P0C7U0, P0CG37, P51693, Q03157, Q29016, Q2F7Z7, Q3T0Q2, Q3UPI1, Q4W8E7, Q5EGE1, Q5PQX1, Q61137, Q68BL7, Q68BL8, Q6H9L7, Q6UWH4, Q766D5, Q76KP1, Q80Z10

Diamond homologs: Q29016, Q3V140, Q60485, Q6AY33, Q8NEB7

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic4
Likely pathogenic0
Uncertain significance72
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (4)

Variant IDHGVSClassification
146024GRCh38/hg38 12p13.33-13.31(chr12:45740-6945196)x3Pathogenic
563988GRCh37/hg19 12p13.33-13.31(chr12:191242-8122785)x3Pathogenic
625811GRCh37/hg19 12p13.33-13.31(chr12:189216-8185497)Pathogenic
685635GRCh37/hg19 12p13.33-13.31(chr12:173786-8393815)x3Pathogenic

SpliceAI

1485 predictions. Top by Δscore:

VariantEffectΔscore
12:6639033:CAAAT:Cacceptor_gain1.0000
12:6639051:C:CTacceptor_gain1.0000
12:6640338:GATAC:Gdonor_loss1.0000
12:6640339:ATAC:Adonor_loss1.0000
12:6640340:TA:Tdonor_loss1.0000
12:6640341:A:Cdonor_loss1.0000
12:6640342:C:CGdonor_loss1.0000
12:6640518:CAGAC:Cacceptor_gain1.0000
12:6640524:T:Gacceptor_loss1.0000
12:6643537:A:ACdonor_gain1.0000
12:6643538:C:CCdonor_gain1.0000
12:6643538:CCGA:Cdonor_gain1.0000
12:6643541:A:ACdonor_gain1.0000
12:6643542:C:CCdonor_gain1.0000
12:6643544:T:TAdonor_gain1.0000
12:6643545:C:Adonor_gain1.0000
12:6643564:T:TAdonor_gain1.0000
12:6643577:T:TAdonor_gain1.0000
12:6644129:T:TAdonor_gain1.0000
12:6644362:T:TAdonor_gain1.0000
12:6644367:AGT:Adonor_gain1.0000
12:6644367:AGTC:Adonor_gain1.0000
12:6644367:AGTCC:Adonor_gain1.0000
12:6644371:C:Adonor_gain1.0000
12:6644376:T:TAdonor_gain1.0000
12:6644380:T:TAdonor_gain1.0000
12:6644383:T:Adonor_gain1.0000
12:6644384:C:Adonor_gain1.0000
12:6644392:C:Adonor_gain1.0000
12:6644395:T:TAdonor_gain1.0000

AlphaMissense

3544 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
12:6640108:C:AW459C0.999
12:6640108:C:GW459C0.999
12:6646523:A:CF106C0.999
12:6646532:A:CF103C0.999
12:6646540:A:CF100L0.999
12:6646540:A:TF100L0.999
12:6646541:A:CF100C0.999
12:6646542:A:GF100L0.999
12:6646813:G:CN81K0.999
12:6646813:G:TN81K0.999
12:6646894:C:AW54C0.999
12:6646894:C:GW54C0.999
12:6638990:T:AK491N0.998
12:6638990:T:GK491N0.998
12:6640110:A:GW459R0.998
12:6640110:A:TW459R0.998
12:6646508:C:GC111S0.998
12:6646509:A:TC111S0.998
12:6646512:G:TR110S0.998
12:6646523:A:GF106S0.998
12:6646531:G:CF103L0.998
12:6646531:G:TF103L0.998
12:6646533:A:GF103L0.998
12:6646568:C:GC91S0.998
12:6646569:A:TC91S0.998
12:6646571:A:TV90D0.998
12:6646817:T:AE80V0.998
12:6638324:C:AW530C0.997
12:6638324:C:GW530C0.997
12:6638979:C:GC495S0.997

dbSNP variants (sampled 300 via entrez): RS1000674503 (12:6639706 G>A,T), RS1000853958 (12:6638475 G>A,T), RS1000855335 (12:6646642 GGAC>G), RS1000945614 (12:6643163 G>A), RS1001125348 (12:6646377 G>A,C), RS1001531832 (12:6649421 C>A), RS1002287378 (12:6643999 G>A), RS1002290280 (12:6637599 C>G,T), RS1002854948 (12:6643469 A>C), RS1002982979 (12:6649302 G>A), RS1003075502 (12:6639931 A>G,T), RS1003240234 (12:6641884 CA>C,CAA), RS1003289096 (12:6645556 T>G), RS1003313500 (12:6648066 C>G), RS1003389025 (12:6638532 A>G)

Disease associations

OMIM: gene MIM:608352 | disease phenotypes: MIM:218340, MIM:615122, MIM:202370

GenCC curated gene-disease

Mondo (4): temtamy syndrome (MONDO:0009033), lymphoproliferative syndrome 2 (MONDO:0014054), peroxisome biogenesis disorder 2B (MONDO:0008736), brain neoplasm (MONDO:0021211)

Orphanet (3): Temtamy syndrome (Orphanet:1777), Combined immunodeficiency due to CD27 deficiency (Orphanet:238505), Neonatal adrenoleukodystrophy (Orphanet:44)

HPO phenotypes

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

GWAS associations

0 associations (top):

MeSH disease descriptors (1)

DescriptorNameTree numbers
C536959Temtamy syndrome (supp.)

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

23 total (human), top 23 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects cotreatment, decreases expression4
aristolochic acid Iincreases expression1
methylmercuric chloridedecreases expression1
triphenyl phosphateaffects expression1
bisphenol Aaffects cotreatment, increases methylation1
di-n-butylphosphoric acidaffects expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
erastinincreases expression1
abrineincreases expression1
dorsomorphinaffects cotreatment, decreases expression1
theaflavin-3,3’-digallateaffects expression1
Fulvestrantincreases methylation, affects cotreatment1
Acetaminophenincreases expression1
Arsenicaffects methylation1
Benzo(a)pyreneaffects methylation, increases methylation1
Endosulfanincreases expression1
Estradioldecreases expression1
Indomethacinincreases expression1
Phthalic Acidsincreases methylation1
Smokedecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Antirheumatic Agentsdecreases expression1
Okadaic Aciddecreases expression1

Clinical trials (associated diseases)

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

TrialPhaseStatusTitle
NCT00075166PHASE4COMPLETEDSurgery Versus Radiosurgery to Treat Metastatic Brain Tumors
NCT00336531PHASE4COMPLETEDEfficacy of Prophylactic Itraconazole in High-Dose Chemotherapy and Autologous Hematopoietic Stem Cell Transplantation
NCT00395863PHASE4COMPLETEDMultihance at 3 Tesla (3T) in Brain Tumors
NCT00415467PHASE4TERMINATEDTreatment of Resectable Malignant Brain Tumors
NCT00576472PHASE4COMPLETEDLearning Impairments Among Survivors of Childhood Cancer
NCT00952081PHASE4COMPLETEDA Pilot Study to Evaluate Efficacy and Safety of Clevidipine in Neurosurgical Patients
NCT02057367PHASE4COMPLETEDScalp Nerve Block and Opioid Consumption in Brain Surgery
NCT02334722PHASE4COMPLETED1 Week Versus 6 Weeks of Levetiracetam in Surgical Brain Tumor Patients
NCT02558569PHASE4COMPLETEDThe Use of Fentanyl in General Anesthesia for Craniotomy With or Without 0.5% Levobupivacaine Scalp Block
NCT02670161PHASE4ENROLLING_BY_INVITATIONQuality Improvement and Practice Based Research in Neurology Using the EMR
NCT02713087PHASE4COMPLETEDVasopressor Effects in Anesthetized Patients
NCT02810899PHASE4COMPLETEDDexmedetomidine and Intelligence Development in Pediatric Patients Undergoing Craniotomy
NCT02964416PHASE4COMPLETEDSingle Dose Tramadol Effect on Extubation Response and Quality of Emergence Post-supratentorial Intracranial Surgery
NCT04266665PHASE4COMPLETEDEffect of Dexmedetomidine on Brain Homeostasis and Neurocognitive Outcome
NCT04313374PHASE4COMPLETEDIntegrated Pulmonary Index and Opioid Based Patient Controlled Analgesia
NCT05141877PHASE4UNKNOWNInfluences of Propofol and Sevoflurane Anesthesia in Brain Tumor
NCT05202899PHASE4UNKNOWNEffect of Sugammadex for Reversal of Rocuronium-induced Neuromuscular Block on Perioperative Management of Awake Craniotomy
NCT05926336PHASE4RECRUITINGThe Effects of Using Different Anesthetics on the Prognosis of Primary Tumors and Its Mechanism of Action
NCT00002875PHASE3COMPLETEDRadiation Therapy Plus Combination Chemotherapy in Treating Children With Medulloblastoma
NCT00002944PHASE3COMPLETEDCombination Chemotherapy in Treating Children With Progressive Brain Tumors
NCT00045968PHASE3UNKNOWNStudy of a Drug [DCVax®-L] to Treat Newly Diagnosed GBM Brain Cancer
NCT00054795PHASE3COMPLETEDStudy of Neurologic Progression With Motexafin Gadolinium and Radiation Therapy (SMART)
NCT00078988PHASE3COMPLETEDHigh-Dose Chemotherapy Plus Autologous Stem Cell Transplantation Compared With Intermediate-Dose Chemotherapy Plus Autologous Stem Cell Transplantation With or Without Isotretinoin in Treating Young Patients With Recurrent High-Grade Gliomas
NCT00085098PHASE3COMPLETEDRadiation Therapy Compared With Chemotherapy and Radiation Therapy in Treating Patients With Newly Diagnosed Primary Central Nervous System (CNS) Germ Cell Tumor
NCT00088166PHASE3COMPLETEDXERECEPT® (hCRF) for Patients Requiring Dexamethasone to Treat Edema Associated With Brain Tumors
NCT00124761PHASE3COMPLETEDA Trial Comparing Radiosurgery With Surgery for Solitary Brain Metastases
NCT00135876PHASE3COMPLETEDDalteparin Low Molecular Weight Heparin for Primary Prophylaxis of Venous Thromboembolism in Brain Tumour Patients
NCT00138788PHASE3COMPLETEDBrain Metastases Study: Radiotherapy Fractionation Schemes in the Treatment of Brain Metastases
NCT00181350PHASE3COMPLETEDSerial CT Scans in Fractionated Stereotactic Radiotherapy
NCT00226655PHASE3COMPLETEDAn Open-Labeled, Extended-Use of XERECEPT (hCRF) for Patients in Studies NTI 0302, 0303, or Other Designated Studies
NCT00226668PHASE3WITHDRAWNXERECEPT® (hCRF) for Primary Glioma Patients Requiring Dexamethasone to Treat Peritumoral Brain Edema
NCT00241670PHASE3COMPLETEDFluorescence-guided Resection of Malignant Gliomas With 5-Aminolevulinic Acid
NCT00280475PHASE3COMPLETEDA Trial of Postoperative Whole Brain Radiation Therapy vs. Salvage Stereotactic Radiosurgery Therapy for Metastasis
NCT00369785PHASE3COMPLETEDDonepezil in Treating Patients Who Have Undergone Radiation Therapy for Brain Tumors
NCT00418691PHASE3TERMINATEDEffects of Methylphenidate Versus Sustained Release Methylphenidate on Cognitive Functioning
NCT00681551PHASE3COMPLETEDMagnevist (SH L 451A) Intra-individual Dose Comparison Study in Patients With Brain Metastasis
NCT00716976PHASE3COMPLETEDSodium Thiosulfate in Preventing Hearing Loss in Young Patients Receiving Cisplatin for Newly Diagnosed Germ Cell Tumor, Hepatoblastoma, Medulloblastoma, Neuroblastoma, Osteosarcoma, or Other Malignancy
NCT01601314PHASE3COMPLETEDPerioperative Magnesium Sulphate as a Cerebral Protector in Neurosurgical Patients
NCT01655927PHASE3UNKNOWNEfficacy of Tranexamic Acid in Brain Tumor Resections
NCT02667587PHASE3COMPLETEDAn Investigational Immuno-therapy Study of Temozolomide Plus Radiation Therapy With Nivolumab or Placebo, for Newly Diagnosed Patients With Glioblastoma (GBM, a Malignant Brain Cancer)