The Dr. Susan Love Foundation for Breast Cancer Research’s mission is to end breast cancer. It challenges the status quo to end breast cancer and improve the lives of people impacted by it now through education and advocacy. The Foundation drives collaborative, cutting-edge research with nontraditional partners, brings to light the collateral damage of treatment and seeks ways to diminish it, and interprets science to empower patients. Fast, flexible, and project-based, the Foundation actively engages the public in scientific research to ensure that it produces accurate and meaningful results. For the past 20 years, Dr. Love has dedicated her career to the eradication of breast cancer and pioneered some of the world’s more innovative research. From spearheading a partnership with NASA’s Jet Propulsion Laboratory to mapping the breast ductal system to harnessing the power of artificial intelligence to develop a handheld, self-reading ultrasound for breast cancer screening in underserved populations. For more information please visit https://drsusanloveresearch.org/
“While the origin of breast cancer is still not well understood, we do know a few things,” stated Dr. Love. “Each breast is comprised of six to 12 duct-lobule units that develop from one or a few stem cells at the time of puberty. In the vast majority of cases, when a woman gets breast cancer it is one and only one of those units; the rest of the breast is without disease. It was on the basis of this understanding that, years ago, I began to envision treatments that focused on the ‘sick duct’ only. Over the years a number of clinical trials have been conducted that demonstrate this approach leads to strong tumor treatment effects, because of the local delivery, and reduced systemic exposure, which hopefully produces fewer side effects. I am pleased that Atossa Genetics and a leading institution are carrying on the research I began and I look forward to advising on this important clinical trial.”
Today, Atossa Genetics Inc. (NASDAQ: ATOS), a clinical-stage biopharmaceutical company developing novel therapeutics and delivery methods for breast cancer and other breast conditions, and The Dr. Susan Love Research Foundation, announced that the Institutional Review Board (IRB) has approved a Phase 2 clinical study of Atossa’s intraductal microcatheter technology for the administration of fulvestrant in patients with early-stage breast cancer or ductal carcinoma in situ (DCIS). Susan Love, M.D., inventor of the technology, will advise Atossa as it conducts the trial. Atossa also entered into a clinical trial agreement with a major research university named in the 8k filing that Atossa filed on 10-14-2019 to conduct their Phase 2 clinical study of Atossa’s intraductal microcatheter technology for the administration of fulvestrant in patients with early-stage breast cancer or ductal carcinoma in situ (DCIS). Atossa Genetics is the owner of issued patents, pending patent applications, and medical device FDA 510(k) premarket notifications related to the treatment of breast conditions, including breast cancer and DCIS.
“We have contracted with a world-class teaching, research, and healthcare organization based in the United States to conduct this study,” commented Steven C. Quay, Ph.D., M.D., CEO and President of Atossa. “Atossa’s intraductal technology was invented by Dr. Love and subsequently acquired by Atossa. We are honored that Dr. Love has agreed to work with us on this important new study. This work begins as Atossa increases its corporate focus on its proprietary Endoxifen for the reduction of mammographic breast density.”
Atossa’s Intraductal Breast Cancer Treatment: The Phase 2 Study
Fulvestrant is FDA-approved for metastatic breast cancer. It is administered as a monthly intramuscular injection of two injections, typically into the buttocks. The AstraZeneca branded drug, Faslodex, had worldwide sales of over $1 billion US in 2018.
This trial is a Phase 2 study in women with Stage 1 or 2 breast cancer (invasive ductal carcinoma) or DCIS scheduled for mastectomy or lumpectomy within 14 to 45 days. This study will assess the safety, tolerability, cellular activity and distribution of fulvestrant when delivered directly into breast milk ducts via Atossa’s intraductal technology, compared to those who receive the same drug by injection. Of the 30 patients required for full enrollment, six will receive the standard intramuscular injection of fulvestrant and 24 will receive fulvestrant with Atossa’s intraductal technology.
The primary endpoint of the clinical trial is to compare the safety, tolerability, and distribution of fulvestrant between the two routes of administration (intramuscular injection or through Atossa’s intraductal technology). The secondary endpoint of the study is to determine if there are changes in the expression of Ki67 as well as estrogen and progesterone receptors between pre-fulvestrant biopsy and post-fulvestrant surgical specimens. Digital breast imaging before and after drug administration in both groups will also be performed to determine the effect of fulvestrant on any lesions as well as breast density of the participant. This Phase 2 study is currently underway at Montefiore Medical Center, which will transition all future work to the new study site.
Additional information can be found in Atossa SEC filings at:
Additional information can be found on the NIH website at: