14/06 Menarini Group and Stemline Therapeutics, Inc. Reports Data from the Phase 3 SENTRY Trial of Selinexor Plus Ruxolitinib in Myelofibrosis CI
28/05 The Menarini Group and Stemline Therapeutics, Inc. Presents New Data From The Phase 1b/2 ELEVATE Study Of Elacestrant In Combination With Capivasertib In Patients With ER+, HER2- Metastatic Breast Cancer CI
25/05 Menarini Group Announces New Data At the American Society of Clinical Oncology 2026 Annual Meeting CI
09/12 Menarini Group and Stemline Therapeutics, Inc. Presents Elacestrant Phase 2 Combination Data in Patients with ER+, HER2- Metastatic Breast Cancer at the 2025 San Antonio Breast Cancer Symposium CI
24/11 Menarini Group and Stemline Therapeutics, Inc. to Present New Data Related to ELZONRIS CI
20/25/20 Menarini Group and Stemline Therapeutics Inc. Announce Collaboration with VisualDx to Aid in Identifying People Who May Have Blastic Plasmacytoid Dendritic Cell Neoplasm CI
12/24/12 Menarini Group Along with Stemline Therapeutics, Inc and Medsir Present the Phase III Study Adela CI
11/23/11 Menarini Group Presents Initial Safety and Efficacy Data from Phase 1B/2 Elevate and Electra Combination Studies of Orserdu® (Elacestrant) in Patients with Er+, Her2- Metastatic Breast Cancer At the 2023 San Antonio Breast Cancer Symposium CI
08/23/08 Menarini Group and Stemline Therapeutics, Inc. Presents New Progression-Free Survival Data from Emerald Clinical Study of Orserdu (Elacestrant) in Clinically Relevant Subgroups of Patients with Esr1 Mutations At Sabcs 2023 CI
21/23/21 The Menarini Group and Stemline Therapeutics, Inc. to Present New Data Related to ORSerDU CI
30/23/30 Quantum Leap Healthcare Collaborative Initiates Landmark Phase 2 RECAST DCIS Platform Trial to Evaluate Alternative DCIS Treatments with Atossa Therapeutics, Havah Therapeutics, and the Menarini Group CI
20/23/20 European Commission Approves Menarini Group?s ORSERDU (Elacestrant) for the Treatment of Patients with ER+, HER2- Locally Advanced or Metastatic Breast Cancer with an Activating ESR1 Mutation CI
26/23/26 The Menarini Group and Stemline Therapeutics Announce Results from A New Analysis of the Pivotal EMERALD Clinical Study CI
Manager TitleAgeSince
Chief Executive Officer 60 -
Director of Finance/CFO 65 16/01/2014
Chief Tech/Sci/R&D Officer - 01/01/2021
Date Insider Type Main position Quantity % Market Cap. Importance
10/06/20 Free

Chief Executive Officer

38,72,092 7.3739%
10/06/20 Tender

Executive/Senior Manager

2,50,891 0.4778%
10/06/20 Tender

Director

1,51,450 0.2884%
Change 5-day change 1-year change 3-year change Capi.($)
-.--%-.--% - - 57Cr
-0.21%-4.43%+44.40%+74.13% 6.62TCr
+0.82%+5.41%+8.05%+73.53% 5.52TCr
-0.22%+6.53%+11.68%+87.32% 5.28TCr
+3.28%+5.58%+26.51%+50.05% 4.55TCr
+0.51%+9.95%+22.40%+133.92% 4.39TCr
-1.15%+0.39%+263.21%+594.60% 4.16TCr
+0.10%+9.90%+16.11%+59.33% 3.4TCr
-7.13%-5.67%+28.08%-0.59% 2.58TCr
+0.69%+5.60%+36.60%+26.94% 2.35TCr
Average -0.33%+4.74%+50.78%+122.14% 4.32TCr
Weighted average by Cap. -0.05%+4.56%+49.62%+126.42%
Logo Stemline Therapeutics, Inc.
Stemline Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on discovering, acquiring, developing and commercializing oncology therapeutics. The Company is developing approximately three clinical stage product candidates, including SL-401, SL-701 and SL-801. SL-401 is a targeted therapy directed to the interleukin-3 receptor (IL-3R) (CD123), present on a range of hematologic cancers. SL-401 consists of IL-3 recombinantly fused to a truncated diphtheria toxin payload. SL-701 is an immunotherapy designed to activate the immune system to attack tumors. SL-701 comprises various short synthetic peptides that correspond to epitopes of targets, including IL-13 receptor subunit alpha-2 (IL-13Ra2), ephrin type-A receptor 2 (EphA2) and survivin, present on brain cancer. SL-801 is an oral, small molecule that reversibly inhibits Exportin-1 (XPO1), also known as Chromosome Region Maintenance-1 (CRM-1), a nuclear transport protein.
Employees
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