Be, Poland
- Featured
We are currently recruiting patients with Palmoplantar Pustulosis (PPP). This study investigates the Efficacy and safety of ANB019.
Visit our website for more information: [_**www.pustulardermstudies.com**_](https://ppp.pustulardermstudies.com/patient/qualify/?media_label=centerwatch)
Phase
2Span
Sponsor
Overland Park, Kansas
Recruiting
- Featured
Arise 2 - A Study of Oral BTD-001 in Adults With Idiopathic Hypersomnia
Stimulant use is allowed if certain criteria are met. 4 or 5 non-consecutive overnight sleep tests may be required.
Phase
2Span
Sponsor
Lenexa, Kansas
Recruiting
Pivotal 2 Study of RGX-314 Gene Therapy in Participants With nAMD
This randomized, partially masked, controlled, Phase 3 clinical study will evaluate the efficacy and safety of ABBV-RGX-314 gene therapy in participants with nAMD. The study will evaluate 2 dose levels of RGX-314 gene therapy relative to an active comparator. The primary endpoint of this study is mean change in best-corrected visual acuity (BCVA) of ABBV-RGX-314 relative to aflibercept. Approximately 660 participants who meet the inclusion/exclusion criteria, will be enrolled into one of 3 arms.
Phase
3Span
257 weeksSponsor
AbbVieLenexa, Kansas
Recruiting
Study of Zifibancimig in Participants With Neovascular Age-Related Macular Degeneration
Phase
1/2Span
374 weeksSponsor
Hoffmann-La RocheLenexa, Kansas
Recruiting
Pivotal 1 Study of ABBV-RGX-314 (Also Known as RGX-314) Gene Therapy Administered Via Subretinal Delivery One Time in Participants With nAMD
This randomized, partially masked, active-controlled, Phase 2b/3 clinical study will evaluate the efficacy and safety of ABBV-RGX-314 gene therapy in participants with nAMD. The study will evaluate 2 dose levels of ABBV-RGX-314 relative to an active comparator. The primary endpoint of this study is the mean change from baseline in best-corrected visual acuity (BCVA) of ABBV-RGX-314 relative to ranibizumab at Week 54. Approximately 540 participants who meet the inclusion/exclusion criteria, will be enrolled into one of 3 arms.
Phase
2/3Span
283 weeksSponsor
AbbVieLenexa, Kansas
Recruiting
A Study to Evaluate Efficacy, Safety & Pharmacokinetics of the Port Delivery System (PDS) With Ranibizumab in Participants With Diabetic Macular Edema (DME) Compared With Intravitreal Ranibizumab; A Subtudy to Evaluate the Safety of Re-Implanting the PDS With Ranibizumab in Participants With DME
Phase
3Span
372 weeksSponsor
Hoffmann-La RocheLenexa, Kansas
Recruiting
Triple Negative Breast Cancer and Germline Hereditary Breast and Ovarian Cancer Mutation Carrier Registry
This study is being done to collect cancer-related information from patients with triple negative breast cancer and patients with hereditary genetic mutations. This information will help us better understand the link between genetic changes and cancer outcome in patients with triple negative breast cancer.
Phase
N/ASpan
772 weeksSponsor
University of Kansas Medical CenterOverland Park, Kansas
Recruiting
Healthy Volunteers
Canakinumab in the Treatment of Acute Gout Flares and Prevention of New Flares in Patients Unable to Use NSAIDs and/or Colchicine.
Phase
3Span
Sponsor
Novartis PharmaceuticalsOverland Park, Kansas
Recruiting
HER2-positive Breast Cancer Registry
Phase
N/ASpan
1049 weeksSponsor
Priyanka SharmaOverland Park, Kansas
Recruiting
A 2-year Study of EYP-1901 in Subjects With Wet Age Related Macular Degeneration (wAMD) (LUGANO) Primary Efficacy Will be Determined at Week 56
Phase
3Span
149 weeksSponsor
EyePoint Pharmaceuticals, Inc.Lenexa, Kansas
Recruiting