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SGN-15

Phase 2

Non-Small Cell Lung Carcinoma | Small molecule | Oncology |Pfizer, Inc.|Trials Updated: Oct 24, 2011

SGN-15 development status

Highest phase Phase 2
Registered trials 2 across 1 sponsor since Jan 2003

SGN-15 target and mechanism

ModalitySmall molecule

Also known as SGN-15 (cBR96-doxorubicin immunoconjugate)

Success Probability

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Market & Valuation

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Trial Design

RandomizedUNCONTROLLED
Total Trials3
Total Enrollment250

FDA Designations

No designations recorded

SGN-15 clinical trials

SGN-15 · 3 trials · 3 indications

Phase 2 3
NCT00086333FDG-PET to Investigate SGN-15 and Docetaxel in Patients With Advanced Non-Small Cell Lung CarcinomaNon-Small Cell Lung Carcinoma
COMPLETED30 Analytics
NCT00031187Study of SGN-15, Antibody-Drug Conjugate, to Treat Hormone Refractory Prostate CancerProstatic Neoplasms
COMPLETED160 Analytics
NCT00051571Safety/Efficacy Study of Immunoconjugate With Docetaxel in Non-small Cell Lung CarcinomaCarcinoma, Non-Small-Cell Lung
COMPLETED60 Analytics
PHASE2COMPLETED
FDG-PET to Investigate SGN-15 and Docetaxel in Patients With Advanced Non-Small Cell Lung Carcinoma
Non-Small Cell Lung CarcinomaUnlock trial analytics
PHASE2COMPLETED
Study of SGN-15, Antibody-Drug Conjugate, to Treat Hormone Refractory Prostate Cancer
Prostatic NeoplasmsUnlock trial analytics
PHASE2COMPLETED
Safety/Efficacy Study of Immunoconjugate With Docetaxel in Non-small Cell Lung Carcinoma
Carcinoma, Non-Small-Cell LungUnlock trial analytics

Study Design & Arms

AllocationRANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeTREATMENT

Interventions

NameTypeDescription
SGN-15, DocetaxelDRUG -
SGN-15 (cBR96-doxorubicin immunoconjugate)DRUG -
Taxotere (docetaxel)DRUG -
SGN-15DRUG -
DocetaxelDRUG -
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Eligibility Criteria

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

Inclusion Criteria: * Patients with pathologically confirmed stage IIIB or IV NSCLC with a minimum of 1 measurable baseline target lesion who have received no prior chemotherapy for metastatic disease and are not eligible for combined modality therapy with curative intent * Patients must have an EC...

Countries:United States
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Frequently asked questions about SGN-15

What is SGN-15 used for?

SGN-15 was studied in oncology for the treatment of non-small cell lung carcinoma and prostatic neoplasms, specifically hormone refractory prostate cancer. It was evaluated in Phase 2 clinical trials in combination with docetaxel. Both indications were investigated in adult patient populations in the United States.

Who is developing SGN-15?

SGN-15 was developed by Pfizer, Inc., which trades under the ticker PFE. The company sponsored the Phase 2 clinical program evaluating the agent in non-small cell lung carcinoma and prostate cancer. All listed trials for SGN-15 are completed.

What phase is SGN-15 in?

SGN-15 is in Phase 2 development. It is an investigational agent and is not approved. Three Phase 2 trials have been completed, and no trials are currently active. The studies enrolled a total of 160 patients across non-small cell lung carcinoma and prostatic neoplasms.

What clinical trials is SGN-15 in?

SGN-15 has been evaluated in three completed Phase 2 trials: NCT00086333, which used FDG-PET to investigate SGN-15 and docetaxel in advanced non-small cell lung carcinoma; NCT00051571, a safety and efficacy study of the immunoconjugate with docetaxel in non-small cell lung carcinoma; and NCT00031187, which studied SGN-15 in hormone refractory prostate cancer.

Is SGN-15 the same as cBR96-doxorubicin immunoconjugate?

Yes, SGN-15 is also known as cBR96-doxorubicin immunoconjugate. It is an antibody-drug conjugate that combines the cBR96 antibody with the chemotherapy agent doxorubicin. The agent has also been studied in combination with docetaxel in clinical trials.

What is SGN-15 used for in non-small cell lung carcinoma?

SGN-15 was studied in non-small cell lung carcinoma as a treatment combined with docetaxel. Two completed Phase 2 trials, NCT00086333 and NCT00051571, evaluated the immunoconjugate in patients with advanced non-small cell lung carcinoma. Both studies were conducted in the United States in adults aged 18 years and older.