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SGN-40

Phase 1

Multiple Myeloma | Small molecule | Oncology |Roche Holding AG|Last Updated: Dec 12, 2022

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment18

FDA Designations

No designations recorded

Clinical trial landscape

SGN-40 · 2 trials · 2 indications

Phase 1 2
NCT00664898A Study of the Safety and Pharmacology of SGN-40 Administered in Combination With Bortezomib in Patients With Relapsed or Refractory Multiple MyelomaMultiple Myeloma
COMPLETED18 Analytics
NCT00556699A Study of SGN-40 in Combination With Rituximab in Patients With CD20-Positive, Follicular and Marginal Zone B-Cell Non-Hodgkin's LymphomaNon-Hodgkin's Lymphoma
COMPLETED22 Analytics
PHASE1COMPLETED
A Study of the Safety and Pharmacology of SGN-40 Administered in Combination With Bortezomib in Patients With Relapsed or Refractory Multiple Myeloma
Multiple MyelomaUnlock trial analytics
PHASE1COMPLETED
A Study of SGN-40 in Combination With Rituximab in Patients With CD20-Positive, Follicular and Marginal Zone B-Cell Non-Hodgkin's Lymphoma
Non-Hodgkin's LymphomaUnlock trial analytics

Study Endpoints

Primary Endpoints

Determine the maximum tolerated dose of SGN-40 when combined with bortezomib
Length of study
Incidence and nature of dose-limiting toxicities in order to determine the maximum tolerated dose
Length of study

Secondary Endpoints

Determine safety, pharmacokinetics, and clinical response rate for combination therapy with SGN-40 and bortezomib
Length of study
Changes in vital signs, physical examination findings, and clinical laboratory results
Length of study
Incidence, nature, and severity of adverse events
Length of study
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Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
1EXPERIMENTAL -

Interventions

NameTypeDescription
bortezomibDRUGEscalating intravenous repeating dose
SGN-40DRUGEscalating intravenous repeating dose
rituximabDRUGEscalating intravenous repeating dose
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo

Inclusion Criteria: * Age ≥ 18 years * Documented pathologic diagnosis of multiple myeloma that has relapsed or failed to respond after treatment with at least one prior systemic therapy (other than corticosteroid monotherapy) * Measurable disease * At least one prior systemic therapy other than si...

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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 SGN-40

What is SGN-40 used for?

SGN-40 is an investigational oncology drug being studied for the treatment of Multiple Myeloma and Non-Hodgkin's Lymphoma. It is currently in Phase 1 clinical development and has not been approved by regulatory authorities.

Who makes SGN-40?

SGN-40 is being developed by Roche Holding AG, which trades under the ticker RHHBY. The drug is in Phase 1 clinical development for oncology indications.

What phase is SGN-40 in?

SGN-40 is in Phase 1 clinical development. It is an investigational drug and has not been approved for any use. Clinical trials for the drug have been completed.

What clinical trials is SGN-40 in?

SGN-40 has been studied in two completed Phase 1 clinical trials. NCT00556699 evaluated SGN-40 in combination with rituximab in patients with CD20-positive follicular and marginal zone B-cell Non-Hodgkin's Lymphoma. NCT00664898 studied SGN-40 in combination with bortezomib in patients with relapsed or refractory Multiple Myeloma.

Is SGN-40 the same as any other drug?

SGN-40 is also known by other names, though specific alternative names have not been disclosed. It is an investigational drug being developed by Roche Holding AG for the treatment of Multiple Myeloma and Non-Hodgkin's Lymphoma.