MedPath

Commons, Marty

🇺🇸United States
Ownership
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Employees
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Market Cap
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Website

A PMS of Jakavi® in Patients With Steroid-Refractory Graft-versus-Host Disease (SR-GvHD) in Korea

Recruiting
Conditions
Graft-versus-Host Disease
Interventions
Other: ruxolitinib
First Posted Date
2022-11-18
Last Posted Date
2025-01-14
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
127
Registration Number
NCT05621733
Locations
🇰🇷

Novartis Investigative Site, Taegu, Korea, Republic of

French Study to Highlight the Unmet Treatment Needs of 3L+ CP-CML and With T315I-mutated CML Patients

Completed
Conditions
Chronic Myeloid Leukemia
Interventions
Other: T315I
Other: 3L Therapy
First Posted Date
2022-11-17
Last Posted Date
2022-11-17
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
200
Registration Number
NCT05619978
Locations
🇫🇷

Novartis Investigative Site, Lyon, France

Sacubitril/Valsartan Treated Adult Patients With Chronic Heart Failure

Completed
Conditions
Chronic Heart Failure
Interventions
First Posted Date
2022-11-14
Last Posted Date
2022-11-15
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
9230
Registration Number
NCT05613140
Locations
🇺🇸

Novartis Investigative Site, East Hanover, New Jersey, United States

Clinical Outcomes of 3L+ Therapies Among Patients With Chronic Myeloid Leukemia and Those With T315I Mutation

Completed
Conditions
Chronic Myeloid Leukemia
First Posted Date
2022-11-09
Last Posted Date
2023-04-06
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
164
Registration Number
NCT05611216
Locations
🇺🇸

Novartis Investigative Site, East Hanover, New Jersey, United States

Treatment Patterns and Outcomes of Targeted Therapy and Immunotherapy Among BRAF-Positive Melanoma Patients Treated in the Adjuvant Setting and Among BRAF-Positive Metastatic Melanoma Patients With Low Tumor Burden

Completed
Conditions
Metastatic Melanoma
Interventions
Combination Product: Dabrafenib+Trametinib
Combination Product: Ipilimumab+Nivolumab
Combination Product: Vemurafenib+Cobimetinib
Combination Product: Encorafenib+Binimetinib
First Posted Date
2022-11-09
Last Posted Date
2023-04-06
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
1975
Registration Number
NCT05611229
Locations
🇺🇸

Novartis Investigative Site, East Hanover, New Jersey, United States

Pharmacokinetics and Safety Study of Siremadlin (HDM201) in Participants With Mild, Moderate and Severe Hepatic Impairment

Phase 1
Completed
Conditions
Hepatic Impairment
Interventions
First Posted Date
2022-10-31
Last Posted Date
2025-05-18
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
38
Registration Number
NCT05599932
Locations
🇺🇸

Texas Liver Institute, San Antonio, Texas, United States

🇺🇸

Clinical Pharmacology of Miami LLC, Miami, Florida, United States

🇺🇸

Orlando Clinical Research Center, Orlando, Florida, United States

A Study to Investigate the Safety, Tolerability and Preliminary Efficacy of NGI226 Microparticles in Patients With Achilles Tendinopathy

Phase 2
Recruiting
Conditions
Achilles Tendinopathy
Interventions
Drug: Placebo
First Posted Date
2022-10-25
Last Posted Date
2025-04-22
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
46
Registration Number
NCT05592990
Locations
🇺🇸

Tucson Orthopedic Institute, Tucson, Arizona, United States

🇺🇸

Advanced Research LLC, Deerfield Beach, Florida, United States

🇺🇸

Houston Methodist Hospital, Houston, Texas, United States

and more 1 locations

Secukinumab Global MAP Cohort for Adult Patients With Hidradenitis Suppurativa (HS)

Conditions
Hidradenitis Suppurativa (HS)
First Posted Date
2022-10-18
Last Posted Date
2023-10-25
Lead Sponsor
Novartis Pharmaceuticals
Registration Number
NCT05583604

Characterization of Early Patients Initiating Ofatumumab for Treatment of Multiple Sclerosis.

Completed
Conditions
Multiple Sclerosis
Interventions
Other: Ofatunumab
First Posted Date
2022-10-13
Last Posted Date
2022-11-08
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
2101
Registration Number
NCT05576779
Locations
🇺🇸

Novartis Investigative Site, East Hanover, New Jersey, United States

A 24-week Study Evaluating the Effectiveness and Safety of Lucentis® 0.2mg in Retinopathy of Prematurity Participants in China

Completed
Conditions
Retinopathy of Prematurity
Interventions
Other: Ranibizumab
First Posted Date
2022-10-13
Last Posted Date
2025-03-25
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
62
Registration Number
NCT05576792
Locations
🇨🇳

Novartis Investigative Site, Guangzhou, Guangdong, China

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