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Active clinical trials for "Giant Cell Tumors"

Results 21-30 of 41

A Study of PLX73086 in Advanced Solid Tumors and Locally Advanced or Refractory Tenosynovial Giant...

Solid TumorsTenosynovial Giant Cell Tumor2 more

The purpose of this research study is to evaluate safety, pharmacokinetics and preliminary efficacy of the investigational drug PLX73086 in subjects with solid tumors including subjects with locally advanced or refractory tenosynovial giant cell tumor (TGCT).

Terminated28 enrollment criteria

Phase 1 Study of PLX7486 as Single Agent in Patients With Advanced Solid Tumors

Solid TumorTumors of Any Histology With Activating Trk (NTRK) Point or NTRK Fusion Mutations1 more

The objective of this study is to determine the safety, pharmacokinetics, maximum tolerated dose/recommended Phase 2 dose, and efficacy of PLX7486.

Terminated21 enrollment criteria

Reduced Dose-density of Denosumab for Unresectable GCTB

Bone Giant Cell Tumor

This study is a multi-center, multi-national, open label, single arm phase 2 study of single-agent denosumab. The objective of the trial is to evaluate the risk versus benefit of denosumab in maintenance setting in patients requiring long-term use (> 1 year) of denosumab. For that purpose, the treatment schedule with reduced dose density (120mg SC 12-weekly instead of 4-weekly) will be investigated, starting after 1-year (12-15 months) of denosumab full dose, as per current label. The impact on OsteoNecrosis of the Jaw (ONJ) without compromising disease control will be assessed.

Terminated35 enrollment criteria

Study of the Effect of Zoledronate on Local Recurrence After Surgical Treatment of Giant Cell Tumors...

Giant Cell Tumors of Bone

The giant cell tumor (GTC) is an aggressive benign bone tumor, growing at the metaphyseal-epiphyseal regions of long bones, especially around the knee and the distal radius.It is responsible for bony destruction in para-articular zone fracture and leading to the breakdown and destruction of the underlying joint. Histologically, the tumor cell contains a contingent of monocytic cells round, a contingent of giant type cell of type osteoclastic responsible for bone resorption that accompanies these tumors and a contingent of lengthened cells fibroblast-like considered to be contingent tumor. The treatment is exclusively surgical; or by resection of the lesion which takes away tumour and its environment, solution which, if it prevents local recurrence, imposes an important bony and articular reconstruction, always limited and deteriorating rapidly over time in these young patients; or by curettage of lesion, by "hollowing-out" of the bone, creating a hole which it will be necessary to fill up by a bony grafting or a substitute of the bone (cement). This last solution, if it preserves a better function, exposes at risk of local recurrence,putting into play the prognosis of articulation near, most often the knee.Despite different local adjuvants treatments used during surgical operation, after having curetted the cavity and before filling it up, the recidivism rates vary from 12 % to 41 % (average 25 %) in literature. The beneficial effect of the adjuvants therapeutics suggests the concept broadly accepted by a tumoral microscopic residual at the origin of the local recidivism .Biphosphonates (BP) is molecules which settle in vivo on the hydroxyapatite of the bone; they inhibit the recruitment of the osteoclast forerunners and the activity of mature osteoclast. Besides, biphosphonates containing some nitrogen (N-BP), leads to the apoptose of mature osteoclast. These molecules also have a direct effect on tumor cells , causing apoptosis of neoplastic cells of myeloma, of breast cancer. Clinical controlled studies confirm the experimental data of N-BP. Two work also showed their effect on osteoclasts and stroma cells of tumours with giant cells but no clinical study assessed potential on the prevention of the local recurrence. The investigators offer a study phase 2 of the effectiveness of N-BP (acid zoledronique) on the prevention of the local recurrence of tumours with primary huge cells after surgical treatment by curettage - filing by a surgeon referent in oncologic orthopedic surgery. Number of patients: 24

Terminated13 enrollment criteria

Adjuvant Zoledronic Acid in High Risk Giant Cell Tumour of Bone (GCT)

Giant Cell Tumor of BoneOsteoclastoma

This is a multicenter, randomised phase II trial in patients with high risk GCT. Primary objective: Determine if adjuvant zoledronic acid improves the 2 years recurrence rate of 'high risk' GCT as compared to standard care Secondary objectives: Determine the relapse free survival Evaluate the usefulness of bone remodelling markers in diagnosing and monitoring GCT

Terminated20 enrollment criteria

Study of Cabiralizumab in Patients With Pigmented Villonodular Synovitis / Diffuse Type Tenosynovial...

Pigmented Villonodular SynovitisTenosynovial Giant Cell Tumor

This is a phase 1/2 single arm, open-label, safety, tolerability, and PK study of cabiralizumab in PVNS/dt-TGCT patients.

Completed13 enrollment criteria

Study to Evaluate Discontinuation and Re-Treatment in Participants With Tenosynovial Giant Cell...

Tenosynovial Giant Cell Tumor

This study is designed to evaluate the discontinuation/re-treatment of pexidartinib therapy in previously treated participants with tenosynovial giant cell tumor (TGCT).

Completed8 enrollment criteria

Safety and Efficacy Study of Denosumab in Patients With Recurrent or Unresectable Giant Cell Tumor...

GCTGiant Cell Tumor of Bone

To determine how safe and effective denosumab is in treating patients with giant cell tumor of bone.

Completed10 enrollment criteria

Study of Denosumab in Subjects With Giant Cell Tumor of Bone

CancerGiant Cell Tumors2 more

To determine how safe denosumab is in treating subjects with giant cell tumor of bone (GCTB)

Completed23 enrollment criteria

MCS110 in Patients With Pigmented Villonodular Synovitis (PVNS)

Pigmented Villonodular SynovitisPVNS4 more

This study, designed as a proof of concept study of MCS110 in pigmented villonodular synovitis, assessed the clinical response to MCS110 treatment in Pigmented Villonodular Synovitis (PVNS) patients, after a single or multiple intravenous doses of MCS110, using magnetic resonance imaging to assess tumor volume, and evaluated the pharmacokinetics/pharmacodynamics, safety and tolerability in this population.

Completed17 enrollment criteria

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