Last reviewed · How we verify

Sr-89

Peking Union Medical College Hospital · FDA-approved active Small molecule

Strontium-89 is a beta-emitting radioisotope that localizes to areas of increased bone metabolism and delivers targeted radiation to relieve bone pain in patients with skeletal metastases.

Strontium-89 is a beta-emitting radioisotope that localizes to areas of increased bone metabolism and delivers targeted radiation to relieve bone pain in patients with skeletal metastases. Used for Bone pain palliation in patients with skeletal metastases from cancer (prostate cancer, breast cancer, and other malignancies with bone involvement).

At a glance

Generic nameSr-89
Also known asstrontium-89 chloride
SponsorPeking Union Medical College Hospital
Drug classRadiopharmaceutical; beta-emitting radioisotope
TargetBone hydroxyapatite (calcium analog); osteoblasts in areas of increased bone metabolism
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Sr-89 is taken up by osteoblasts in bone lesions due to its chemical similarity to calcium. Once localized to sites of increased bone turnover (such as metastatic lesions), it emits beta particles that deliver high local radiation dose to the tumor and surrounding bone tissue, causing pain relief. The mechanism provides palliative benefit by destroying metastatic bone lesions and reducing osteoclastic activity.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: