- What Parents Need to Know About Teens and Concussions
- Beware of Hand Sanitizers Containing Methanol
- What Athletes Should Know About COVID-19, Heart Damage and Working Out
- Will a Cheap Pill Cure Gonorrhea? New Test Can Tell
- Model Shows 300,000 American Deaths by December if More Don’t Wear Face Masks
- Health Highlights: Aug. 7, 2020
- Men’s Genital Bacteria Help Predict Partners’ Risk for Vaginal Infection: Study
- Will Your Kid Play School Sports This Fall? Here’s Some Guidance on Doing It Safely
- Many Older Adults Can’t Connect With Telehealth: Study
- Many Older Americans Getting Cancer Screens They Don’t Need: Study
Xgeva Approved for Rare, Non-Malignant Tumor
THURSDAY, June 13Xgeva (denosumab) has been approved by the U.S. Food and Drug Administration to treat giant cell tumor of the bone (GCTB), a rare tumor that’s most often non-cancerous.
The tumor usually affects adults between ages 20 and 40, although it may also develop in adolescents, the FDA said Thursday in a news release. It typically doesn’t spread, although in rare cases it can become cancerous and travel to the lungs.
As a non-cancerous tumor, GCTB destroys bone as it becomes larger, causing pain, fractures and loss of mobility. Xgeva has been approved in cases where the tumor can’t be surgically removed, or might lead to a severe outcome such as loss of a limb, the agency said.
Xgeva, approved under the FDA’s expedited review program, was evaluated for this use in two clinical trials involving a total of 305 adults and adolescents. Common side effects included joint pain, headache, nausea, fatigue, back pain and extremity pain.
Women of childbearing potential should use “highly effective” contraception while taking Xgeva, since the drug can harm a fetus, the FDA warned.
The drug was first approved in 2010 to prevent fractures when cancer has spread to the bone. It’s marketed by Amgen, based in Thousand Oaks, Calif.
More information
The FDA has more about this approval.
Source: HealthDay
