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ABT-751

Phase 2

Breast Cancer | Small molecule | Oncology |Abbott Laboratories|Trials Updated: Nov 29, 2007

ABT-751 development status

Highest phase Phase 2
Registered trials 6 across 2 sponsors since Jun 2003

ABT-751 target and mechanism

Molecular targetTUBB4B, TUBB1, TUBB3, TUBB4A, TUBB8, TUBB
Target classInhibitor
ModalitySmall molecule

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLED
Total Trials4
Total Enrollment170

FDA Designations

No designations recorded

ABT-751 clinical trials

ABT-751 · 4 trials · 4 indications

Phase 2 4
NCT00073151A Study of ABT-751 in Patients With Non-Small Cell Lung CancerNon-Small Cell Lung Cancer
COMPLETED30 Analytics
NCT00073112A Study of ABT-751 in Patients With Renal Cell CancerRenal Cell Cancer
COMPLETED60 Analytics
NCT00073138A Study of ABT-751 in Patients With Colorectal CancerColorectal Cancer
COMPLETED40 Analytics
NCT00063102A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol or Taxotere) Therapy.Breast Cancer
COMPLETED40 Analytics
PHASE2COMPLETED
A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer
Non-Small Cell Lung CancerUnlock trial analytics
PHASE2COMPLETED
A Study of ABT-751 in Patients With Renal Cell Cancer
Renal Cell CancerUnlock trial analytics
PHASE2COMPLETED
A Study of ABT-751 in Patients With Colorectal Cancer
Colorectal CancerUnlock trial analytics
PHASE2COMPLETED
A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol or Taxotere) Therapy.
Breast CancerUnlock trial analytics

Study Endpoints

Primary Endpoints

Objective Response Rate in subjects with NSCLC
1 year
Objective Response Rate in subjects with RCC
1 year
Objective Response Rate in subjects with Recurrent Colorectal Cancer
1 year
Objective Response Rate in subjects with Breast cancer
1 year

Secondary Endpoints

Time to Tumor Progression (TTP)
1 year
Survival
2 years
Toxicities associated with treatment administration
1 year
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Interventions

NameTypeDescription
ABT-751DRUG -
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites17

Inclusion Criteria * Stage IIIB or IV non-small cell lung cancer. * Recurrent tumor following treatment with paclitaxel or docetaxel. * Able to tolerate normal activities of daily living. * Adequate bone marrow, kidney and liver function. Exclusion Criteria * Pregnant or breast feeding. * Anti-tu...

Countries:United StatesCanada
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Competitive Landscape -Breast Cancer 609 trials

Frequently asked questions about ABT-751

What is ABT-751 used for?

ABT-751 is an investigational oral small molecule that has been studied in several solid tumor types: non-small cell lung cancer, colorectal cancer, renal cell cancer, and recurrent breast cancer after taxane therapy. It is not an approved therapy; all clinical work to date has been in Phase 2 trials in oncology.

What does ABT-751 target?

ABT-751 targets tubulin, binding the beta-tubulin subunits TUBB1, TUBB3, TUBB4A, TUBB4B, TUBB8, and TUBB. It acts as a tubulin inhibitor, interfering with microtubule dynamics in dividing cells. This mechanism is distinct from that of taxanes, which also act on tubulin but at a different binding site.

Who is developing ABT-751?

ABT-751 was developed by Abbott Laboratories, which trades on the New York Stock Exchange under the ticker ABT. Abbott sponsored the Phase 2 clinical program evaluating the compound across multiple solid tumor indications in the United States and Canada.

What phase is ABT-751 in?

ABT-751 is in Phase 2 development. Four Phase 2 studies have been completed, and no active trials are currently recruiting. The compound has not been approved by the FDA for any indication and remains investigational.

What clinical trials is ABT-751 in?

ABT-751 has been evaluated in four completed Phase 2 trials: NCT00073151 in non-small cell lung cancer, NCT00073138 in colorectal cancer, NCT00073112 in renal cell cancer, and NCT00063102 in recurrent breast cancer after taxane therapy. All were uncontrolled, non-randomized studies conducted in the United States, with the renal cell trial also including sites in Canada.

Is ABT-751 the same as combretastatin?

No. ABT-751 is a distinct small molecule tubulin inhibitor developed by Abbott Laboratories. It is not the same compound as combretastatin or other tubulin-binding agents, and it has its own ChEMBL identifier, CHEMBL20684.