Conexxence (denosumab-bnht) is a prescription medication approved by the U.S. Food and Drug Administration (FDA) to treat osteoporosis in women after menopause who are at high risk for fracture. It is also approved to increase bone mass in men with osteoporosis who are at high risk for fracture.
Conexxence is a type of osteoporosis treatment called a RANK ligand (RANKL) inhibitor. It blocks a protein called RANKL that helps control cells that break down bone. By blocking this protein, Conexxence slows bone breakdown and helps increase bone mass and strength.
Conexxence is a biosimilar of Prolia. This means it is made from living cells and is designed to work like the original medicine. The FDA requires biosimilars to have no meaningful differences in safety or how well they work.
Doctors prescribe Conexxence when:
Conexxence is given as an injection under the skin by a healthcare provider.
The recommended dose of Conexxence is 60 milligrams given as an injection under the skin once every six months.
People receiving Conexxence should also take 1,000 milligrams of calcium each day and at least 400 international units of vitamin D each day.
This information is based on prescribing information, but your healthcare provider may tailor your treatment plan. Always follow their guidance.
In clinical studies of denosumab, the active ingredient in Prolia, the reference product for Conexxence, the most common side effects differed depending on why people were taking it.
In women with osteoporosis after menopause, common side effects include:
In men with osteoporosis, common side effects include:
In people with glucocorticoid-induced osteoporosis, common side effects include:
In people with bone loss related to certain prostate or breast cancer treatments, side effects include:
Conexxence can cause serious side effects that may require immediate medical attention. These include:
Get medical help right away if you think you are having a serious reaction.
Fresenius Kabi, the manufacturer of Conexxence, offers the KabiCare Patient Support Program.
The KabiCare Patient Support Program offers help enrolling in KabiCare, navigating insurance coverage and financial assistance, accessing medication, learning about your disease, injection training, and refill reminders.
To learn more, visit Conexxence support resources or call 833-522-4227.
Before you start Conexxence:
Tell your doctor if you have any allergies to denosumab-bnht or any ingredients in Conexxence.
Tell your doctor about all medicines you take, including prescription drugs, over-the-counter medicines, vitamins, and herbal supplements.
Also tell your doctor if you:
Take good care of your teeth and gums while receiving Conexxence. Brush and floss regularly, and tell your dentist that you receive Conexxence before having dental work.
Do not receive Conexxence if you:
Conexxence is also FDA-approved to increase bone mass in men at high risk for fracture who are receiving androgen deprivation therapy for prostate cancer that has not spread to other parts of the body. It is also approved to increase bone mass in women at high risk for fracture who are receiving adjuvant aromatase inhibitor therapy as part of breast cancer care.
If you miss a dose, get the injection as soon as possible. After that, your next dose should be scheduled six months from the date of your last injection.
Do not receive Conexxence if you are pregnant because it may cause fetal harm. If you can become pregnant, use effective birth control during treatment and for at least five months after your last dose. Tell your doctor right away if you become pregnant during treatment.
If you are breastfeeding or plan to breastfeed, tell your doctor. It is not known if Conexxence passes into breast milk. You should not receive Conexxence and breastfeed at the same time.
These answers are fact-checked by our editorial staff.
How effective is Conexxence for osteoporosis?
In a three-year study of women with osteoporosis after menopause:
In a separate one-year study of men with osteoporosis:
How long does Conexxence take to work for osteoporosis?
Studies of denosumab found that its effects on bone breakdown began soon after treatment. A marker of bone breakdown called serum type 1 C-telopeptide decreased by about 85 percent within three days. The largest decreases were seen by month 1.
At years 1, 2, and 3, denosumab significantly reduced new spine fractures in women with osteoporosis after menopause. It also increased bone mineral density at the bone sites measured after three years. The studies do not say exactly when a person will notice Conexxence working.
Should I take Conexxence for osteoporosis if I have an infection?
Conexxence may increase the risk of serious infections. These can include infections of the skin, abdomen, urinary tract, or ear.
People who take medicines that weaken the immune system, or who already have a weakened immune system, may have a higher risk of serious infections. Your doctor should consider the benefits and risks of Conexxence before treatment.
If you develop a serious infection while receiving Conexxence, your doctor should decide whether you should continue treatment. Get medical care promptly if you develop signs or symptoms of a serious infection, including cellulitis, which is a serious skin infection.
On MyOsteoTeam, people share their experiences with osteoporosis, get advice, and find support from others who understand.
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