MedPath

Proparacaine

Generic Name
Proparacaine
Brand Names
Alcaine, Lenalidomide Krka d.d. Novo mesto (previously Lenalidomide Krka), Revlimid, Lenalidomide Mylan, Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto), Lenalidomide Accord
Drug Type
Small Molecule
Chemical Formula
C16H26N2O3
CAS Number
499-67-2
Unique Ingredient Identifier
B4OB0JHI1X
Background

Proparacaine is a topical anesthetic drug of the amino ester group. It is found in ophthalmic solutions at a concentration of 0.5% as the hydrochloride salt.

Indication

Used as a local (ophthalmic) anesthetic.

Associated Conditions
Chronic Lymphocytic Leukemia (CLL) - Refractory, Follicular Lymphoma ( FL), Mantle Cell Lymphoma (MCL), Marginal Zone Lymphoma (MZL), Multiple Myeloma (MM), Myelodysplastic Syndrome, Primary Amyloidosis, Refractory Diffuse Large B Cell Lymphoma (DLBCL)
Associated Therapies
Local Anaesthesia therapy

Safety and Efficacy of Single-agent CC-5013 in Subjects With Relapsed and Refractory Multiple Myeloma

Phase 2
Completed
Conditions
Multiple Myeloma
Interventions
First Posted Date
2003-07-23
Last Posted Date
2019-11-12
Lead Sponsor
Celgene
Target Recruit Count
222
Registration Number
NCT00065351
Locations
🇺🇸

Providence St. Joseph Medical Center/Cancer Center, Burbank, California, United States

🇺🇸

Massachusetts General Hospital, Boston, Massachusetts, United States

🇺🇸

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

and more 21 locations

Lenalidomide Safety/Efficacy in Myelodysplastic Syndromes (MDS) Associated With a Deletion (Del)(5q) Cytogenetic Abnormality

Phase 2
Completed
Conditions
Myelodysplastic Syndromes
Interventions
First Posted Date
2003-07-18
Last Posted Date
2019-11-19
Lead Sponsor
Celgene
Target Recruit Count
148
Registration Number
NCT00065156
Locations
🇺🇸

Arizona Cancer Center, Tucson, Arizona, United States

🇺🇸

Desert Hematology & Oncology Medical Group, Rancho Mirage, California, United States

🇺🇸

Mayo Clinic, Rochester, Minnesota, United States

and more 26 locations

Efficacy and Safety Study of CC-5013 Monotherapy in Subjects With Myelodysplastic Syndromes

Phase 2
Completed
Conditions
Myelodysplastic Syndromes
Interventions
First Posted Date
2003-07-17
Last Posted Date
2013-04-04
Lead Sponsor
Celgene Corporation
Target Recruit Count
215
Registration Number
NCT00064974
Locations
🇺🇸

Alta Bates Cancer Center, Berkeley, California, United States

🇺🇸

Midwest Cancer Research Group, Skokie, Illinois, United States

🇺🇸

The Cleveland Clinic Foundation, Cleveland, Ohio, United States

and more 113 locations

S0232 Dexamethasone With or Without Lenalidomide in Treating Patients With Previously Untreated Stage I, Stage II, or Stage III Multiple Myeloma

Phase 3
Completed
Conditions
Plasma Cell Neoplasm
Multiple Myeloma
Interventions
First Posted Date
2003-07-09
Last Posted Date
2015-03-25
Lead Sponsor
SWOG Cancer Research Network
Target Recruit Count
198
Registration Number
NCT00064038
Locations
🇺🇸

William Beaumont Hospital - Royal Oak Campus, Royal Oak, Michigan, United States

🇺🇸

Utah Cancer Specialists at UCS Cancer Center, Salt Lake City, Utah, United States

Study to Compare the Efficacy and Safety of CC-5013 vs. Placebo in Subjects With Metastatic Malignant Melanoma.

Phase 3
Completed
Conditions
Melanoma
Neoplasm Metastasis
First Posted Date
2003-04-08
Last Posted Date
2019-11-08
Lead Sponsor
Celgene
Target Recruit Count
274
Registration Number
NCT00057616
Locations
🇦🇺

Royal Newcastle Hospital, Newcastle, New South Wales, Australia

🇦🇺

Westmead Hospital, Westmead, New South Wales, Australia

🇦🇺

Royal Hobart Hospital, Hobart, Tasmania, Australia

and more 46 locations

CC-5013 Plus Dexamethasone Versus Dexamethasone Alone in Previously Treated Subjects With Multiple Myeloma

Phase 3
Completed
Conditions
Multiple Myeloma
Interventions
First Posted Date
2003-03-07
Last Posted Date
2017-10-19
Lead Sponsor
Celgene
Target Recruit Count
353
Registration Number
NCT00056160
Locations
🇺🇸

Ohio State University, Columbus, Ohio, United States

🇺🇸

MD Anderson Cancer Center, Houston, Texas, United States

🇺🇸

Clinical Research Consultants, Inc., Hoover, Alabama, United States

and more 46 locations

CC-5013 in Treating Patients With Cancer That Has Not Responded to Previous Therapy

Phase 1
Completed
Conditions
Lymphoma
Small Intestine Cancer
Unspecified Adult Solid Tumor, Protocol Specific
First Posted Date
2003-01-27
Last Posted Date
2012-03-15
Lead Sponsor
National Institutes of Health Clinical Center (CC)
Registration Number
NCT00031941
Locations
🇺🇸

NCI - Center for Cancer Research, Bethesda, Maryland, United States

🇺🇸

Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support, Bethesda, Maryland, United States

CC-5013 in Treating Patients With Recurrent Glioma

Phase 1
Completed
Conditions
Brain and Central Nervous System Tumors
First Posted Date
2003-01-27
Last Posted Date
2015-04-30
Lead Sponsor
National Cancer Institute (NCI)
Registration Number
NCT00036894
Locations
🇺🇸

Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support, Bethesda, Maryland, United States

A Phase II Study of Continuous Versus Syncopated Dosing of CC-5013 for the Treatment of Refractory Multiple Myeloma

Phase 2
Completed
Conditions
Multiple Myeloma
First Posted Date
2003-01-07
Last Posted Date
2009-09-23
Lead Sponsor
Celgene Corporation
Target Recruit Count
100
Registration Number
NCT00051116
Locations
🇺🇸

Myeloma Institute University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States

Phase 1 Study OF CDC-501 in Patients With Solid Tumors

Phase 1
Completed
Conditions
Neoplasms
Interventions
First Posted Date
2002-10-03
Last Posted Date
2019-11-18
Lead Sponsor
Celgene
Target Recruit Count
24
Registration Number
NCT00046735
Locations
🇺🇸

Wake Forest University, Winston-Salem, North Carolina, United States

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