Matching articles for "Orserdu"
Camizestrant (Etcamah) for Advanced Breast Cancer
The Medical Letter on Drugs and Therapeutics • October 26, 2026; (Issue 1766)
Camizestrant (Etcamah – AstraZeneca), an oral estrogen
receptor antagonist, has received accelerated approval from
the FDA for use in combination with a cyclin-dependent
kinase (CDK) 4/6 inhibitor for...
Camizestrant (Etcamah – AstraZeneca), an oral estrogen
receptor antagonist, has received accelerated approval from
the FDA for use in combination with a cyclin-dependent
kinase (CDK) 4/6 inhibitor for treatment of hormone
receptor (HR)-positive, human epidermal growth factor
receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer in adults who have ESR1 mutations that were
detected in circulating tumor DNA (ctDNA) during treatment
with an aromatase inhibitor and a CDK 4/6 inhibitor.
Vepdegestrant (Veppanu) for Advanced Breast Cancer
The Medical Letter on Drugs and Therapeutics • July 20, 2026; (Issue 1759)
Vepdegestrant (Veppanu – Rigel), an oral heterobifunctional
protein degrader, has been approved by the FDA for treatment
of estrogen receptor (ER)-positive, human epidermal growth
factor receptor 2...
Vepdegestrant (Veppanu – Rigel), an oral heterobifunctional
protein degrader, has been approved by the FDA for treatment
of estrogen receptor (ER)-positive, human epidermal growth
factor receptor 2 (HER2)-negative, estrogen receptor 1
(ESR1)-mutated advanced or metastatic breast cancer
in adults who had disease progression following ≥1 prior
line of endocrine therapy. It is the first proteolysis targeting
chimera (PROTAC), a type of heterobifunctional protein
degrader, to be approved in the US. The oral selective
estrogen receptor degraders (SERDs) elacestrant (Orserdu)
and imlunestrant (Inluriyo) were approved earlier for the
same indication.
Imlunestrant (Inluriyo) for Advanced Breast Cancer
The Medical Letter on Drugs and Therapeutics • January 19, 2026; (Issue 1746)
The FDA has approved imlunestrant (Inluriyo – Lilly),
an oral estrogen receptor antagonist, for treatment
of estrogen receptor (ER)-positive, human epidermal
growth factor receptor 2 (HER2)-negative,...
The FDA has approved imlunestrant (Inluriyo – Lilly),
an oral estrogen receptor antagonist, for treatment
of estrogen receptor (ER)-positive, human epidermal
growth factor receptor 2 (HER2)-negative, estrogen
receptor 1 (ESR1)-mutated advanced or metastatic
breast cancer in adults who had disease progression
following at least one prior line of endocrine therapy.
Imlunestrant is the second oral selective estrogen
receptor degrader (SERD) to be approved in the US for
treatment of breast cancer; elacestrant (Orserdu) was
approved in 2023.
Elacestrant (Orserdu) for Advanced or Metastatic Breast Cancer
The Medical Letter on Drugs and Therapeutics • March 6, 2023; (Issue 1671)
The FDA has approved elacestrant (Orserdu –
Stemline), an oral estrogen receptor antagonist, for
treatment of estrogen receptor (ER)-positive, human
epidermal growth factor receptor 2...
The FDA has approved elacestrant (Orserdu –
Stemline), an oral estrogen receptor antagonist, for
treatment of estrogen receptor (ER)-positive, human
epidermal growth factor receptor 2 (HER2)-negative,
estrogen receptor 1 (ESR1)-mutated advanced or
metastatic breast cancer in postmenopausal women
or men who had disease progression following
endocrine therapy. Elacestrant is the first oral selective
estrogen receptor degrader (SERD) to be approved
for treatment of breast cancer; the injectable SERD
fulvestrant (Faslodex, and generics) was approved
more than 20 years ago.
