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MFGR1877S

Phase 1

Multiple Myeloma | Small molecule | Oncology |Roche Holding AG|Trials Updated: Nov 2, 2016

MFGR1877S development status

Highest phase Phase 1
Registered trials 2 across 1 sponsor since May 2010

Success Probability

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Market & Valuation

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Trial Design

RandomizedUNCONTROLLED
Total Trials2
Total Enrollment38

FDA Designations

No designations recorded

MFGR1877S clinical trials

MFGR1877S · 2 trials · 2 indications

Phase 1 2
NCT01363024Trial Evaluating the Safety and Pharmacokinetics of MFGR1877S in Patients With Advanced Solid TumorsSolid Tumor
COMPLETED24 Analytics
NCT01122875A Study of the Safety and Pharmacokinetics of MFGR1877S in Patients With Relapsed or Refractory t(4;14)-Positive Multiple MyelomaMultiple Myeloma
COMPLETED14 Analytics
PHASE1COMPLETED
Trial Evaluating the Safety and Pharmacokinetics of MFGR1877S in Patients With Advanced Solid Tumors
Solid TumorUnlock trial analytics
PHASE1COMPLETED
A Study of the Safety and Pharmacokinetics of MFGR1877S in Patients With Relapsed or Refractory t(4;14)-Positive Multiple Myeloma
Multiple MyelomaUnlock trial analytics

Study Endpoints

Primary Endpoints

Incidence of dose dose limiting toxicities (DLTs) by NCI CTCAE, v4.0
Days 1-28 of Cycle 1
Nature of dose limiting toxicities (DLTs) by NCI CTCAE, v4.0
Days 1-28 of Cycle 1
Incidence and nature of dose-limiting toxicities (DLTs)
Throughout study or until early study discontinuation

Secondary Endpoints

Incidence of adverse events by NCI CTCAE, v4.0
Up to 1 year
Nature of adverse events by NCI CTCAE, v4.0
Up to 1 year
Severity of adverse events by NCI CTCAE, v4.0
Up to 1 year
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Study Design & Arms

AllocationRANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
AEXPERIMENTAL -

Interventions

NameTypeDescription
MFGR1877SDRUGIntravenous escalating dose
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites5

Inclusion Criteria: * Life expectancy \>/= 12 weeks * ECOG performance status of 0 or 1 * Histologic or cytologic documentation of locally advanced, or metastatic solid malignancy that has relapsed after or failed to respond to at least one prior regimen or for which there is no standard therapy * ...

Countries:United StatesCanada
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Competitive Landscape -Multiple Myeloma 338 trials

Frequently asked questions about MFGR1877S

What is MFGR1877S used for?

MFGR1877S is an investigational small molecule being studied for the treatment of solid tumors and multiple myeloma. It has been evaluated in Phase 1 clinical trials for these oncology indications, though it is not yet approved and remains in clinical development.

Who makes MFGR1877S?

MFGR1877S is being developed by Roche Holding AG, which trades under the ticker RHHBY. The company has sponsored clinical trials to evaluate the drug's safety and pharmacokinetics in patients with cancer.

What phase is MFGR1877S in?

MFGR1877S is in Phase 1 clinical development. It has completed Phase 1 trials for both solid tumors and multiple myeloma, but it is not approved and is still considered investigational.

What clinical trials is MFGR1877S in?

MFGR1877S has been studied in two completed Phase 1 trials: NCT01122875 for relapsed or refractory t(4;14)-positive multiple myeloma and NCT01363024 for advanced solid tumors. Both trials evaluated safety and pharmacokinetics in adult patients.

Is MFGR1877S the same as another drug?

MFGR1877S is the primary name for this investigational agent. No alternative names have been reported for this drug in the available clinical trial information.