Prochymal, developed by Osiris Therapeutics, is a preparation of mesenchymal stem cells, which are obtained from the bone marrow of healthy young adult donors.
Prochymal, developed by Osiris Therapeutics, is a preparation of mesenchymal stem cells, which are obtained from the bone marrow of healthy young adult donors.
In a small clinical trial, six months of treatment with the drug Zytiga, added to standard therapy, eliminated or nearly eliminated tumors in about one-third of men whose disease had not yet spread beyond the prostate gland.
Some environmental and consumer groups say that increased use of Dow Chemical’s herbicide, 2,4-D, could cause cancer, hormone disruption and other health problems.
A combination of two pills proved extremely effective in a small trial but the two companies who manufacture the pills have not agreed to collaborate, to the chagrin of some doctors.
The Food and Drug Administration approved a new anemia drug called Omontys for dialysis patients, which will end Amgen’s 24-year monopoly led by its Epogen drug.
The University of Pennsylvania filed the suit against Dr. Craig B. Thompson, claiming he improperly used research done at the university to start a pharmaceutical company.
The University of Pennsylvania filed the suit against Dr. Craig B. Thompson, claiming he improperly used research done at the university to start a pharmaceutical company.
The president of Memorial Sloan-Kettering Cancer Center, Dr. Craig B. Thompson, is in a billion-dollar dispute with his former workplace over accusations that he walked away with research.
The president of Memorial Sloan-Kettering Cancer Center, Dr. Craig B. Thompson, is in a billion-dollar dispute with his former workplace over accusations that he walked away with research.
The Food and Drug Administration called Kalydeco a “breakthrough therapy” because it treats the underlying cause of the genetic disease, rather than just the symptoms.
The Food and Drug Administration called Kalydeco a “breakthrough therapy” because it treats the underlying cause of the genetic disease, rather than just the symptoms.
The Food and Drug Administration called Kalydeco a “breakthrough therapy” because it treats the underlying cause of the genetic disease, rather than just the symptoms.
The drug, Erivedge, made by Genentech, was approved for adults with basal cell carcinoma that has spread elsewhere in the body or those who are not candidates for surgery or radiation.
The drug, Erivedge, made by Genentech, was approved for adults with basal cell carcinoma that has spread elsewhere in the body or those who are not candidates for surgery or radiation.
The Food and Drug Administration twice declined to approve Bydureon in 2010, with its most serious concern being that the drug might contribute to heart rhythm abnormalities.
The Food and Drug Administration twice declined to approve Bydureon in 2010, with its most serious concern being that the drug might contribute to heart rhythm abnormalities.
A treatment that improved the vision of two women with forms of macular degeneration could be a breakthrough for regenerative medicine after a recent setback.
Federal drug regulators are seeking more data from AstraZeneca and Bristol-Myers Squibb before deciding whether to approve dapagliflozin, a new drug aimed at Type 2 diabetes.
A new study by the Cochrane Collaboration finds that the Roche drug Tamiflu does not reduce flu complications and transmission as much as previous studies suggested.
The F.D.A. issued guidance to the industry on companion diagnostics in July, including its preference for having the test ready for approval at the same time as the drug.
The F.D.A. issued guidance to the industry on companion diagnostics in July, including its preference for having the test ready for approval at the same time as the drug.
Kevin W. Sharer, the chief executive, and Dr. Roger M. Perlmutter, the head of research, will step down in 2012. The company’s growth has slowed in recent years.
Timothy Brown of San Francisco had two bone-marrow transplants to treat leukemia, and H.I.V. can no longer be detected in his body.The experiences of two patients now suggest to many scientists that a cure may be achievable even if it is years away.
Alnylam Pharmaceuticals says it has developed a drug using the technique of RNA interference that appears to work in people, providing a proof of concept.
The agency said the drug “has not been shown to be safe and effective” for breast cancer patients, but would remain available for treating other types of cancer.
The Food and Drug Administration approved Incyte to be the first drug to treat myelofibrosis, a rare but potentially life-threatening bone marrow disorder.
After doubts about the drug’s efficacy, the Food and Drug Administration is considering whether to rescind approval of it for the treatment of breast cancer.
Five more patients who were being treated with the drug Avastin for eye disease have been blinded, according to one of the patients and medical professionals.
Five more patients who were being treated with the drug Avastin for eye disease have been blinded, according to one of the patients and medical professionals.
Avastin, sold by Genentech, is approved to treat cancer, not eye disease, but many doctors use it because it is many times cheaper than an alternative drug.
As competition for patients and treatments intensifies, more medical centers are offering a controversial procedure in which inner organs are bathed in hot chemotherapy drugs.
As competition for patients and treatments intensifies, more medical centers are offering a controversial procedure in which inner organs are bathed in hot chemotherapy drugs.
As competition for patients and treatments intensifies, more medical centers are offering a controversial procedure in which inner organs are bathed in hot chemotherapy drugs.
As competition for patients and treatments intensifies, more medical centers are offering a controversial procedure in which inner organs are bathed in hot chemotherapy drugs.
In a series of 6-0 votes, an advisory committee to the F.D.A. endorsed the agency’s proposal to revoke the approval of the drug for use against advanced breast cancer.
With breast cancer patients imploring the Food and Drug Administration to change course, the agency’s staff argued that the drug Avastin should lose its approval as a treatment for that disease.
The drugs, mainly for men with late-stage prostate cancer, can extend lives for additional months, but some cost more than $90,000 for a course of treatment.
The drugs, mainly for men with late-stage prostate cancer, can extend lives for additional months, but some cost more than $90,000 for a course of treatment.
The drugs, mainly for men with late-stage prostate cancer, can extend lives for additional months, but some cost more than $90,000 for a course of treatment.
The drug, called Dificid, is the first new medicine in 25 years approved to treat diarrhea caused by Clostridium difficile, a nasty and persistent bacterium.
Induced pluripotent stem cells appear to have the healing potential of embryonic stem cells without the controversy, but when given to mice, they didn’t survive the immune response.
Ricoh, a maker of copiers, swung into action after the March earthquake and has nearly recovered. Japan says 64 percent of damaged factories have bounced back.
The committee has authority to determine which medical devices and procedures the state will cover for its employees, Medicaid patients and injured workers.
Entrepreneurs haven’t yet struck gold in their search for an incision-free procedure to help millions of obese Americans, but it isn’t for lack of effort.