Mavorixafor (DrugBank: -)
1 disease| 告示番号 | 疾患名（ページ内リンク） | 臨床試験数 |
|---|---|---|
| 65 | 原発性免疫不全症候群 | 11 |
| No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | EUCTR2019-001153-10-GB (EUCTR) | 21/12/2020 | 29/06/2020 | A treatment study in patients with WHIM Syndrome. | A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Mavorixafor in Patients with WHIM Syndrome with Open-Label Extension - A treatment study in patients with WHIM Syndrome. | WHIM Syndrome;Therapeutic area: Body processes [G] - Immune system processes [G12] | Product Name: Mavorixafor Product Code: X4P-001 INN or Proposed INN: Mavorixafor | X4 Pharmaceuticals Incorporated | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 28 | Phase 3 | United States;Spain;Turkey;Austria;Russian Federation;Israel;United Kingdom;Italy;France;Hungary;Canada;Poland;Australia;Denmark;Germany;Netherlands;Korea, Republic of | ||
| 2 | EUCTR2019-001153-10-DE (EUCTR) | 20/10/2020 | 26/03/2020 | A treatment study in patients with WHIM Syndrome. | A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Mavorixafor in Patients with WHIM Syndrome with Open-Label Extension - A treatment study in patients with WHIM Syndrome. | WHIM Syndrome;Therapeutic area: Body processes [G] - Immune system processes [G12] | Product Name: Mavorixafor Product Code: X4P-001 INN or Proposed INN: Mavorixafor | X4 Pharmaceuticals Incorporated | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 28 | Phase 3 | United States;Spain;Turkey;Austria;Israel;Russian Federation;United Kingdom;Italy;France;Hungary;Canada;Poland;Australia;Denmark;Germany;Netherlands;Korea, Republic of | ||
| 3 | EUCTR2019-001153-10-AT (EUCTR) | 16/10/2020 | 24/03/2020 | A treatment study in patients with WHIM Syndrome. | A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Mavorixafor in Patients with WHIM Syndrome with Open-Label Extension - A treatment study in patients with WHIM Syndrome. | WHIM Syndrome;Therapeutic area: Body processes [G] - Immune system processes [G12] | Product Name: Mavorixafor Product Code: X4P-001 INN or Proposed INN: Mavorixafor | X4 Pharmaceuticals Incorporated | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 28 | Phase 3 | United States;Spain;Turkey;Austria;Israel;Russian Federation;United Kingdom;Italy;France;Hungary;Canada;Poland;Australia;Denmark;Germany;Netherlands;Korea, Republic of | ||
| 4 | EUCTR2019-001153-10-NL (EUCTR) | 09/09/2020 | 06/04/2020 | A treatment study in patients with WHIM Syndrome. | A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Mavorixafor in Patients with WHIM Syndrome with Open-Label Extension - A treatment study in patients with WHIM Syndrome. | WHIM Syndrome;Therapeutic area: Body processes [G] - Immune system processes [G12] | Product Name: Mavorixafor Product Code: X4P-001 INN or Proposed INN: Mavorixafor | X4 Pharmaceuticals Incorporated | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 28 | Phase 3 | United States;Portugal;Spain;Turkey;Austria;Israel;United Kingdom;Italy;France;Hungary;Canada;Belgium;Poland;Romania;Australia;Denmark;Netherlands;Germany;Korea, Republic of | ||
| 5 | NCT04154488 (ClinicalTrials.gov) | August 15, 2020 | 4/11/2019 | A Study of Mavorixafor in Participants With Severe Congenital Neutropenia and Chronic Neutropenia Disorders | A Phase 1B, Open-Label, Multicenter Study of Mavorixafor in Patients With Severe Congenital Neutropenia and Chronic Neutropenia Disorders | Neutropenia | Drug: Mavorixafor | X4 Pharmaceuticals | NULL | Not yet recruiting | 12 Years | N/A | All | 45 | Phase 1 | United States |
| No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
| 6 | EUCTR2019-001153-10-PL (EUCTR) | 27/04/2020 | 09/03/2020 | A treatment study in patients with WHIM Syndrome. | A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Mavorixafor in Patients with WHIM Syndrome with Open-Label Extension - A treatment study in patients with WHIM Syndrome. | WHIM Syndrome;Therapeutic area: Body processes [G] - Immune system processes [G12] | Product Name: Mavorixafor Product Code: X4P-001 INN or Proposed INN: Mavorixafor | X4 Pharmaceuticals Incorporated | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 28 | Phase 3 | United States;Spain;Turkey;Austria;Israel;Russian Federation;United Kingdom;Italy;France;Hungary;Canada;Poland;Australia;Denmark;Germany;Netherlands;Korea, Republic of | ||
| 7 | EUCTR2019-001153-10-ES (EUCTR) | 02/03/2020 | 02/12/2019 | A treatment study in patients with WHIM Syndrome. | A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Mavorixafor in Patients with WHIM Syndrome with Open-Label Extension - A treatment study in patients with WHIM Syndrome. | WHIM Syndrome;Therapeutic area: Body processes [G] - Immune system processes [G12] | X4 Pharmaceuticals Incorporated | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 28 | Phase 3 | Portugal;United States;Spain;Turkey;Austria;Israel;Italy;United Kingdom;France;Hungary;European Union;Canada;Poland;Belgium;Romania;Australia;Denmark;Netherlands;Germany;Korea, Republic of | |||
| 8 | EUCTR2019-001153-10-HU (EUCTR) | 08/01/2020 | 08/11/2019 | A treatment study in patients with WHIM Syndrome. | A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Mavorixafor in Patients with WHIM Syndrome with Open-Label Extension - A treatment study in patients with WHIM Syndrome. | WHIM Syndrome;Therapeutic area: Body processes [G] - Immune system processes [G12] | X4 Pharmaceuticals Incorporated | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 28 | Phase 3 | Portugal;United States;Spain;Turkey;Austria;Israel;Italy;United Kingdom;France;Hungary;European Union;Canada;Poland;Belgium;Romania;Australia;Denmark;Netherlands;Germany;Korea, Republic of | |||
| 9 | EUCTR2019-001153-10-DK (EUCTR) | 16/12/2019 | 21/10/2019 | A treatment study in patients with WHIM Syndrome. | A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Mavorixafor in Patients with WHIM Syndrome with Open-Label Extension - A treatment study in patients with WHIM Syndrome. | WHIM Syndrome;Therapeutic area: Body processes [G] - Immune system processes [G12] | Product Name: Mavorixafor Product Code: X4P-001 INN or Proposed INN: Mavorixafor | X4 Pharmaceuticals Incorporated | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 28 | Phase 3 | United States;Spain;Turkey;Austria;Israel;Russian Federation;United Kingdom;Italy;France;Hungary;Canada;Poland;Denmark;Australia;Germany;Netherlands;Korea, Republic of | ||
| 10 | NCT03995108 (ClinicalTrials.gov) | October 17, 2019 | 19/6/2019 | Efficacy and Safety Study of Mavorixafor in Participants With Warts, Hypogammaglobulinemia, Infections, and Myelokathexis (WHIM) Syndrome | A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Mavorixafor in Patients With WHIM Syndrome With Open-Label Extension | WHIM Syndrome | Drug: Mavorixafor;Drug: Placebo | X4 Pharmaceuticals | NULL | Recruiting | 12 Years | N/A | All | 28 | Phase 3 | United States;Australia;Austria;Denmark;France;Hungary;Italy;Korea, Republic of;Spain |
| No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
| 11 | NCT03005327 (ClinicalTrials.gov) | December 2016 | 20/12/2016 | A Dose Determination and Safety Study of X4P-001 (Mavorixafor) in Participants With Warts, Hypogammaglobulinemia, Infections, and Myelokathexis (WHIM) Syndrome | A Phase 2, Open-Label, Multi-Center Trial of Mavorixafor in Patients With WHIM Syndrome | WHIM Syndrome | Drug: X4P-001 | X4 Pharmaceuticals | NULL | Active, not recruiting | 18 Years | N/A | All | 15 | Phase 2 | United States;Australia |