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Home / FDA - Page 31

FDA

Genentech drug Xolair (omalizumab) was approved
Biotechnology | Disease | FDA | Therapeutics

Genentech drug Xolair (omalizumab) was approved

On Jun. 20, 2003, Genentech drug Xolair (omalizumab) was approved by the U. S. Food and Drug Administration…

Read More Genentech drug Xolair (omalizumab) was approvedContinue

The FDA approved the drug bortezomib (Velcade) for the treatment of multiple myeloma
FDA | Life Science History

The FDA approved the drug bortezomib (Velcade) for the treatment of multiple myeloma

On May 13, 2003, the FDA approved the drug bortezomib (Velcade) for the treatment of multiple myeloma. In…

Read More The FDA approved the drug bortezomib (Velcade) for the treatment of multiple myelomaContinue

The National Academy of Sciences released “Scientific Criteria to Ensure Safe Food”
Agriculture | Biotechnology | FDA | USDA

The National Academy of Sciences released “Scientific Criteria to Ensure Safe Food”

On Apr. 7, 2003, the National Academy of Sciences released “Scientific Criteria to Ensure Safe Food,” a report…

Read More The National Academy of Sciences released “Scientific Criteria to Ensure Safe Food”Continue

Long-term efficacy and safety of etanercept was found in children with polyarticular-course juvenile rheumatoid arthritis
Biotechnology | Disease | FDA | Medicine | Therapeutics

Long-term efficacy and safety of etanercept was found in children with polyarticular-course juvenile rheumatoid arthritis

On Jan. 10, 2003, long-term efficacy and safety of etanercept (Enbrel) was found in children with polyarticular-course juvenile…

Read More Long-term efficacy and safety of etanercept was found in children with polyarticular-course juvenile rheumatoid arthritisContinue

Two randomized controlled trials showed that taking aspirin daily for as little as three years reduces the development of colorectal polyps
Biotechnology | FDA | Therapeutics

Two randomized controlled trials showed that taking aspirin daily for as little as three years reduces the development of colorectal polyps

In 2003, two randomized controlled trials showed that taking aspirin daily for as little as three years reduces…

Read More Two randomized controlled trials showed that taking aspirin daily for as little as three years reduces the development of colorectal polypsContinue

The FDA Office of Combination Products was formed
FDA | Life Science History

The FDA Office of Combination Products was formed

On Dec. 24, 2002, the FDA’s Office of Combination Products was formed within the Office of the Commissioner,…

Read More The FDA Office of Combination Products was formedContinue

Vaccine that combined diphtheria, tetanus, acellular pertussis, inactivated polio and hepatitis B antigens was licensed
FDA | Infectious Disease | Polio | Vaccine

Vaccine that combined diphtheria, tetanus, acellular pertussis, inactivated polio and hepatitis B antigens was licensed

On Dec. 13, 2002, the U.S. Food and Drug Administration (FDA) announced it had licensed a combined diphtheria…

Read More Vaccine that combined diphtheria, tetanus, acellular pertussis, inactivated polio and hepatitis B antigens was licensedContinue

Genentech drug Pegasys (peginterferon alfa-2a) approved
Biotechnology | Disease | FDA

Genentech drug Pegasys (peginterferon alfa-2a) approved

On Dec. 3, 2002, Genentech drug Pegasys (peginterferon alfa-2a) was approved by the Food and Drug Administration (FDA)…

Read More Genentech drug Pegasys (peginterferon alfa-2a) approvedContinue

NCI and FDA scientists reported patterns of proteins found in patients’ blood can distinguish between prostate cancer and benign conditions
Biotechnology | Diagnostics | FDA | Life Science History | Oncology

NCI and FDA scientists reported patterns of proteins found in patients’ blood can distinguish between prostate cancer and benign conditions

On Oct. 16, 2002, patterns of proteins found in patients’ blood may help distinguish between prostate cancer and…

Read More NCI and FDA scientists reported patterns of proteins found in patients’ blood can distinguish between prostate cancer and benign conditionsContinue

FDA announced initiative to modernize the regulation of pharmaceutical manufacturing
FDA | Life Science History

FDA announced initiative to modernize the regulation of pharmaceutical manufacturing

On Aug. 21, 2002, the FDA announced an initiative to modernize the regulation of pharmaceutical manufacturing and product…

Read More FDA announced initiative to modernize the regulation of pharmaceutical manufacturingContinue

The FDA announced the current good manufacturing practice (cGMP) initiative
FDA | Life Science History

The FDA announced the current good manufacturing practice (cGMP) initiative

On Aug. 21, 2002, the FDA announced an effort to enhance and update the regulation of manufacturing processes…

Read More The FDA announced the current good manufacturing practice (cGMP) initiativeContinue

FDA approved Amgen’s aranesp for anemia associated with chemotherapy
Biotechnology | FDA | Oncology | Therapeutics

FDA approved Amgen’s aranesp for anemia associated with chemotherapy

On Jul. 22, 2002, Amgen announced that the U.S. Food and Drug Administration (FDA) had approved Aranesp (darbepoetin…

Read More FDA approved Amgen’s aranesp for anemia associated with chemotherapyContinue

Immunex Corp. was acquired by Amgen
Biotechnology | FDA | Therapeutics

Immunex Corp. was acquired by Amgen

On Jul. 16, 2002, Amgen completed it’s acquisition of Immunex Corporation for $16 billion in stock and net…

Read More Immunex Corp. was acquired by AmgenContinue

President Bush signed the Public Health Security and Bioterrorism Preparedness and Response Act into law
Biotechnology | Diagnostics | FDA | Infectious Disease | Medicine | NIH | Plague | Radiology | Therapeutics | U.S. Congress

President Bush signed the Public Health Security and Bioterrorism Preparedness and Response Act into law

On Jun. 12, 2002, President George W. Bush signed the Public Health Security and Bioterrorism Preparedness and Response…

Read More President Bush signed the Public Health Security and Bioterrorism Preparedness and Response Act into lawContinue

Diphtheria and tetanus toxoids and acellular pertussis vaccine (Daptacel by Aventis Pasteur) was licensed
FDA | Infectious Disease | Vaccine

Diphtheria and tetanus toxoids and acellular pertussis vaccine (Daptacel by Aventis Pasteur) was licensed

On May 14, 2002, the Food and Drug Administration (FDA) approved for use an additional combined diphtheria and…

Read More Diphtheria and tetanus toxoids and acellular pertussis vaccine (Daptacel by Aventis Pasteur) was licensedContinue

BOTOX(R) cosmetic (onabotulinumtoxinA) approved by the FDA
Biotechnology | FDA | Therapeutics

BOTOX(R) cosmetic (onabotulinumtoxinA) approved by the FDA

On Apr. 15, 2002, BOTOX(R) cosmetic (onabotulinumtoxinA), manufactured by Allergan, was approved by the Food and Drug Administration…

Read More BOTOX(R) cosmetic (onabotulinumtoxinA) approved by the FDAContinue

The FDA approved the first nucleic acid test system to screen whole blood donors for infections with HIV and HCV
FDA | HIV | Life Science History

The FDA approved the first nucleic acid test system to screen whole blood donors for infections with HIV and HCV

On Feb. 28, 2002, the FDA announced it had licensed the first nucleic acid test (NAT) system intended…

Read More The FDA approved the first nucleic acid test system to screen whole blood donors for infections with HIV and HCVContinue

Scientists from NCI and FDA reported that patterns of proteins found in patients’ serum may reflect the presence of ovarian cancer
Biotechnology | Diagnostics | FDA | Oncology

Scientists from NCI and FDA reported that patterns of proteins found in patients’ serum may reflect the presence of ovarian cancer

On Feb. 7, 2002, scientists from the National Cancer Institute (NCI) and the Food and Drug Administration (FDA)…

Read More Scientists from NCI and FDA reported that patterns of proteins found in patients’ serum may reflect the presence of ovarian cancerContinue

FDA approved Gleevec for gastrointestinal stromal tumors treatment
Biotechnology | FDA | Non-Profit Research | Oncology | Therapeutics

FDA approved Gleevec for gastrointestinal stromal tumors treatment

On Feb. 1, 2002, the U.S. Food and Drug Administration (FDA) approved the drug Gleevec, formerly known as…

Read More FDA approved Gleevec for gastrointestinal stromal tumors treatmentContinue

The Best Pharmaceuticals for Children Act improved safety and efficacy of patented and off-patent medicines for children
Diagnostics | FDA | Medicine | Pharmaceutical | Therapeutics

The Best Pharmaceuticals for Children Act improved safety and efficacy of patented and off-patent medicines for children

In 2002, the U.S. Congress passed the Best Pharmaceuticals for Children Act that improved safety and efficacy of…

Read More The Best Pharmaceuticals for Children Act improved safety and efficacy of patented and off-patent medicines for childrenContinue

The acquisition of Immunex by Amgen for $16 billion was announced
Biotechnology | FDA | Medicine | Therapeutics

The acquisition of Immunex by Amgen for $16 billion was announced

On Dec. 17, 2001, the acquisition of Immunex by Amgen was announced for $16 billion in stock and…

Read More The acquisition of Immunex by Amgen for $16 billion was announcedContinue

Genentech drug Cathflo Activase (alteplase) was approved
Biotechnology | Disease | FDA | Therapeutics

Genentech drug Cathflo Activase (alteplase) was approved

On Sept. 13, 2001, the Food and Drug Administration (FDA) announced it had approved Genentech’s  request for it’s…

Read More Genentech drug Cathflo Activase (alteplase) was approvedContinue

The FDA approved Gleevec, developed by OHSU, for treatment of chronic myeloid leukemia
Biotechnology | FDA | Non-Profit Research | Oncology | Therapeutics

The FDA approved Gleevec, developed by OHSU, for treatment of chronic myeloid leukemia

On May 10, 2001, the U.S. Food and Drug Administration (FDA) approved Gleevec, the world’s first targeted cancer…

Read More The FDA approved Gleevec, developed by OHSU, for treatment of chronic myeloid leukemiaContinue

Genentech drug Valcyte (valganciclovir hydrochloride) was approved
Biotechnology | FDA | HIV | Therapeutics

Genentech drug Valcyte (valganciclovir hydrochloride) was approved

On Mar. 29, 2001, the Food and Drug Administration (FDA) announced it had approved Genentech’s drug Valcyte (valganciclovir…

Read More Genentech drug Valcyte (valganciclovir hydrochloride) was approvedContinue

Corus Pharma was incorporated
Biotechnology | Disease | FDA | Pharmaceutical | Therapeutics

Corus Pharma was incorporated

On Jan. 12, 2001, Corus Pharma was incorporated as a private venture-backed development stage biopharmaceutical company focused on…

Read More Corus Pharma was incorporatedContinue

SynCardia Systems was founded
FDA | Medical Device | Therapeutics

SynCardia Systems was founded

In 2001, SynCardia Systems, a private company formed to commercialize the Jarvik 7 artificial heart, was founded by…

Read More SynCardia Systems was foundedContinue

Pathogenesis was acquired by Chiron for $660 million
Biotechnology | Disease | FDA | Life Science History | Therapeutics

Pathogenesis was acquired by Chiron for $660 million

On Sept. 22, 2000, Pathogenesis was acquired by Emeryville, California-based Chiron for $660 million or $38.50 per share….

Read More Pathogenesis was acquired by Chiron for $660 millionContinue

The Supreme Court ruled the FDA does not have authority to regulate tobacco as a drug
Disease | FDA | Oncology | U.S. Congress

The Supreme Court ruled the FDA does not have authority to regulate tobacco as a drug

On Mar. 21, 2000, the Supreme Court ruled 5 to 4 along ideological lines, that the U.S. Food…

Read More The Supreme Court ruled the FDA does not have authority to regulate tobacco as a drugContinue

Eli Lilly and Takeda Chemical Industries launched Actos, an oral antidiabetes agent
Biotechnology | FDA | Therapeutics

Eli Lilly and Takeda Chemical Industries launched Actos, an oral antidiabetes agent

In 2000, Eli Lilly and Takeda Chemical launched Actos, an oral anti diabetes agent. In 2005, a PROactive…

Read More Eli Lilly and Takeda Chemical Industries launched Actos, an oral antidiabetes agentContinue

FDA approved Targretin to treat certain T-cell lymphomas
Biotechnology | FDA | Oncology | Therapeutics

FDA approved Targretin to treat certain T-cell lymphomas

On Dec. 29, 1999, the U.S. Food and Drug Administration (FDA) approved Bexarotene (Targretin) to treat cutaneous T-cell…

Read More FDA approved Targretin to treat certain T-cell lymphomasContinue

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