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A Phase I/II Open-label Study of MCS110 in Patients With Prostate Cancer and Bone Metastases

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Novartis

Status and phase

Terminated
Phase 2
Phase 1

Conditions

Prostate Cancer
Bone Metastases

Treatments

Drug: MCS110

Study type

Interventional

Funder types

Industry

Identifiers

NCT00757757
CMCS110A2101

Details and patient eligibility

About

This study will evaluate the safety and efficacy of MCS110 in patients with prostate cancer and bone metastases

Enrollment

3 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with asymptomatic castrate-resistant prostate cancer with bone metastases who have not received any bisphosphonates in the 12 months prior to enrollment
  • 18 years old and over

Exclusion criteria

  • Plan to be on cytotoxic or biologic therapy during study
  • Active dental problems
  • Active heart complications
  • Active infection
  • Patients with moderate to severe swelling due to fluid

Other protocol-defined inclusion/exclusion criteria may apply

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

3 participants in 1 patient group

MCS110
Experimental group
Treatment:
Drug: MCS110

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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