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CDC-501

Phase 2

Multiple Myeloma | Small molecule | Oncology |Bristol-Myers Squibb Company|Last Updated: Nov 12, 2019

Success Probability

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Market & Valuation

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Trial Design

RandomizedUNCONTROLLED
Total Trials1
Total Enrollment102

FDA Designations

No designations recorded

Clinical trial landscape

CDC-501 · 1 trial · 1 indication

Phase 2 1
NCT00044018CDC-501 Therapy in Relapsed or Refractory Multiple MyelomaMultiple Myeloma
COMPLETED102 Analytics
PHASE2COMPLETED
CDC-501 Therapy in Relapsed or Refractory Multiple Myeloma
Multiple MyelomaUnlock trial analytics

Study Endpoints

Primary Endpoints

Confirmed M-Protein Response During Single Agent CDC-501 Therapy
Response assessed every 4 weeks; up to 62 months

M-Protein response evaluated every 4 weeks through urine and serum electrophoresis.

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Study Design & Arms

AllocationRANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Interventions

NameTypeDescription
CDC-501DRUG -
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites4

* Subject must be diagnosed with multiple myeloma (with measurable M-Protein in serum and/or urine), and be considered to have disease progression after at least two cycles of treatment or have relapsed after treatment. * Subject must understand and voluntarily sign an informed consent document. * S...

Countries:United States
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Competitive Landscape -Multiple Myeloma 221 trials

Top 20 of 25 competitors

CompanyTickerTrialsLead PhaseDrugs
AbbVie, Inc.ABBV16PHASE3Pomalidomide, Dexamethasone, Venetoclax
Bristol-Myers Squibb CompanyBMY18PHASE3Iberdomide, Lenalidomide
Takeda Pharmaceutical Co. Ltd. Sponsored ADRTAK5PHASE3IGI, 10%
GSK plc Sponsored ADRGSK17PHASE3Belantamab mafodotin, Pomalidomide, Dexamethasone, Bortezomib
Johnson & JohnsonJNJ28PHASE3Talquetamab, Pomalidomide, Teclistamab, Elotuzumab, Dexamethasone
Regeneron Pharmaceuticals, Inc.REGN11PHASE3Linvoseltamab, Carfilzomib, Daratumumab, Dexamethasone, Pomalidomide
Pfizer Inc.PFE11PHASE3Elranatamab, Lenalidomide
Sanofi SA Sponsored ADRSNY17PHASE3Isatuximab, Dexamethasone, Pomalidomide, Montelukast, Paracetamol/ Acetaminophen
AstraZeneca PLCAZN5PHASE3AZD0120, Daratumumab, Carfilzomib, Dexamethasone, Bortezomib
Gilead Sciences, Inc.GILD3PHASE3Anitocabtagene Autoleucel, Cyclophosphamide, Fludarabine, Pomalidomide, Bortezomib
Karyopharm Therapeutics, Inc.KPTI6PHASE3Selinexor, Elotuzumab, Pomalidomide, Dexamethasone
Grifols, S.A. Sponsored ADR Class BGRFS1PHASE3Xembify
BioLineRX Ltd. Sponsored ADRBLRX1PHASE3BL-8040/kg, G-CSF
C4 Therapeutics, Inc.CCCC3PHASE2Cemsidomide, Dexamethasone
Cellectar Biosciences, Inc.CLRB1PHASE2Iopofosine I 131 single dose, Iopofosine I 131 fractionated dose
GeoVax Labs, Inc.GOVX1PHASE2COVID-19 Vaccine, Synthetic MVA-based SARS-CoV-2 Vaccine GEO-CM04S1
Autolus Therapeutics Plc Sponsored ADRAUTL1PHASE2AUTO CAR T cell therapy
Incyte CorporationINCY2PHASE1Ruxolitinib, Lenalidomide, Methylprednisolone
Moderna, Inc.MRNA2PHASE1mRNA-2808
BeOne Medicines Ltd. Sponsored ADRONC1PHASE1Sonrotoclax, Dexamethasone, Carfilzomib, Daratumumab, Pomalidomide
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Frequently asked questions about CDC-501

What is CDC-501 used for?

CDC-501 is an investigational small molecule being studied for the treatment of multiple myeloma, a cancer of plasma cells. It is being developed by Bristol-Myers Squibb Company (BMY) and has been evaluated in patients with relapsed or refractory multiple myeloma.

What does CDC-501 target?

CDC-501 is a small molecule therapeutic being investigated for multiple myeloma. Its specific molecular target has not been disclosed in available clinical trial information, so its mechanism of action is not publicly detailed.

Who makes CDC-501?

CDC-501 is being developed by Bristol-Myers Squibb Company, a biopharmaceutical company listed on the New York Stock Exchange under the ticker symbol BMY. The company has conducted clinical research on this investigational drug for multiple myeloma.

What phase is CDC-501 in?

CDC-501 has completed a Phase 2 clinical trial in patients with relapsed or refractory multiple myeloma. The trial, which enrolled 102 participants, was conducted in the United States and has been completed, meaning the drug is no longer in active clinical development according to available records.

What clinical trials is CDC-501 in?

CDC-501 has been studied in one clinical trial, identified as NCT00044018, titled "CDC-501 Therapy in Relapsed or Refractory Multiple Myeloma." This Phase 2 trial enrolled 102 patients with multiple myeloma in the United States and has been completed.

Is CDC-501 FDA approved?

CDC-501 is an investigational drug and is not FDA approved. It has been evaluated in a completed Phase 2 clinical trial for relapsed or refractory multiple myeloma, but no approval status has been established based on available information.