( DrugBank: - )
1 disease
告示番号 | 疾患名(ページ内リンク) | 臨床試験数 |
---|---|---|
276 | 軟骨無形成症 | 46 |
276. 軟骨無形成症
臨床試験数 : 46 / 薬物数 : 29 - (DrugBank : 6) / 標的遺伝子数 : 5 - 標的パスウェイ数 : 30
Showing 1 to 10 of 46 diseases
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 | EUCTR2021-001855-15-ES (EUCTR) | 02/02/2022 | 15/09/2021 | A study to evaluate long-term Infigratinib in children with Achondroplasia | Phase 2, Open-Label, Long-Term, Extension (OLE) Study of Infigratinib, an FGFR 1-3-Selective Tyrosine Kinase Inhibitor, in Children with Achondroplasia: PROPEL OLE - PROPEL OLE Phase 2, Open-Label, Long-Term, Extension (OLE) Study of Infigratinib, an FGFR 1-3-Selective Tyrosin ... | Achondroplasia in Children <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia;System Organ Class: 100000004850;Therapeutic area: Diseases [C] - Musculoskeletal Diseases [C05] Achondroplasia in Children <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Ac ... | Product Name: Infigratinib<br>Product Code: BGJ398 (also known as BBP-831)<br>INN or Proposed INN: INFIGRATINIB Product Name: Infigratinib<br>Product Code: BGJ398 (also known as BBP-831)<br>INN or Proposed INN: I ... | QED Therapeutics, Inc. | NULL | Authorised-recruitment may be ongoing or finished | <an>br>Female: yes Male: yes | 280 | Phase 2 | France;United States;Canada;Spain;Australia;United Kingdom | ||
2 | NCT05246033 (ClinicalTrials.gov) | January 5, 2022 | 9/2/2022 | A Dose Escalation Trial Evaluating Safety, Efficacy, and Pharmacokinetics of Multiple Subcutaneous Doses of TransCon CNP Administered Once Weekly in Children With Achondroplasia A Dose Escalation Trial Evaluating Safety, Efficacy, and Pharmacokinetics of Multiple Subcutaneous D ... | ACcomplisH China: A Phase 2, Multicenter, Randomized, Placebo-controlled, Dose Escalation Trial Evaluating Safety, Efficacy, and Pharmacokinetics of Multiple Subcutaneous Doses of TransCon CNP Administered Once Weekly in Children With Achondroplasia ACcomplisH China: A Phase 2, Multicenter, Randomized, Placebo-controlled, Dose Escalation Trial Eval ... | Achondroplasia | Drug: TransCon CNP;Drug: Placebo for TransCon CNP | Ascendis Pharma A/S | NULL | Recruiting | 2 Years | 10 Years | All | 64 | Phase 2 | China |
3 | EUCTR2021-003149-39-ES (EUCTR) | 14/12/2021 | 17/09/2021 | A PHASE 2 OPEN LABEL EXTENSION STUDY TO ASSESS THE LONG-TERM SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF RECIFERCEPT IN CHILDREN WITH ACHONDROPLASIA A PHASE 2 OPEN LABEL EXTENSION STUDY TO ASSESS THE LONG-TERM SAFETY, TOLERABILITY, PHARMACOKINETICS ... | A PHASE 2 OPEN LABEL EXTENSION STUDY TO ASSESS THE LONG-TERM SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF RECIFERCEPT IN CHILDREN WITH ACHONDROPLASIA A PHASE 2 OPEN LABEL EXTENSION STUDY TO ASSESS THE LONG-TERM SAFETY, TOLERABILITY, PHARMACOKINETICS ... | Achondroplasia <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia;System Organ Class: 100000004850;Therapeutic area: Body processes [G] - Bones and nerves physological processes [G11] Achondroplasia <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia ... | Product Name: Recifercept (proposed INN)<br>Product Code: PF-07256472<br>INN or Proposed INN: Recifercept (proposed INN)<br>Other descriptive name: TA-46 Product Name: Recifercept (proposed INN)<br>Product Code: PF-07256472<br>INN or Proposed INN: Recife ... | Pfizer Inc. | NULL | Authorised-recruitment may be ongoing or finished | <an>br>Female: yes Male: yes | 63 | Phase 2 | Portugal;United States;Belgium;Spain;Denmark;Australia;Italy;Japan | ||
4 | NCT05116046 (ClinicalTrials.gov) | December 7, 2021 | 18/10/2021 | Continuation Study of Long-term Safety, Tolerability, Pharmacokinetics and Efficacy of Recifercept in Achondroplasia Continuation Study of Long-term Safety, Tolerability, Pharmacokinetics and Efficacy of Recifercept i ... | A PHASE 2 OPEN LABEL EXTENSION STUDY TO ASSESS THE LONG-TERM SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF RECIFERCEPT IN CHILDREN WITH ACHONDROPLASIA A PHASE 2 OPEN LABEL EXTENSION STUDY TO ASSESS THE LONG-TERM SAFETY, TOLERABILITY, PHARMACOKINETICS ... | Achondroplasia | Biological: Recifercept | Pfizer | NULL | Not yet recruiting | 15 Months | 12 Years | All | 63 | Phase 2 | NULL |
5 | NCT05145010 (ClinicalTrials.gov) | December 6, 2021 | 22/11/2021 | Extension Study of Infigratinib in Children With Achondroplasia (ACH) | Phase 2, Open-Label, Long-Term, Extension (OLE) Study of Infigratinib, an FGFR 1-3-Selective Tyrosine Kinase Inhibitor, in Children With Achondroplasia: PROPEL OLE Phase 2, Open-Label, Long-Term, Extension (OLE) Study of Infigratinib, an FGFR 1-3-Selective Tyrosin ... | Achondroplasia | Drug: Infigratinib | QED Therapeutics, Inc. | NULL | Recruiting | 3 Years | 18 Years | All | 280 | Phase 2 | Australia;United Kingdom |
6 | EUCTR2020-001189-13-PT (EUCTR) | 26/02/2021 | 29/09/2020 | Phase 2 study of safety, tolerability, PK and efficacy of recifercept in achondroplasia | A PHASE 2 MULTIPLE DOSE, RANDOMIZED STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF RECIFERCEPT IN CHILDREN WITH ACHONDROPLASIA A PHASE 2 MULTIPLE DOSE, RANDOMIZED STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND ... | Achondroplasia <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia;System Organ Class: 100000004850;Therapeutic area: Body processes [G] - Bones and nerves physological processes [G11] Achondroplasia <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia ... | Product Name: Recifercept (proposed INN)<br>Product Code: PF-07256472<br>INN or Proposed INN: Recifercept (proposed INN)<br>Other descriptive name: TA-46 Product Name: Recifercept (proposed INN)<br>Product Code: PF-07256472<br>INN or Proposed INN: Recife ... | Pfizer Inc. | NULL | Authorised-recruitment may be ongoing or finished | <an>br>Female: yes Male: yes | 63 | Phase 2 | United States;Portugal;Spain;Belgium;Denmark;Australia;United Kingdom;Italy;Japan | ||
7 | EUCTR2019-002754-22-PT (EUCTR) | 05/02/2021 | 18/06/2020 | A Phase 2 study to evaluate the safety, efficacy and pharmacokinetics of TransCon CNP in prepubertal children with achondroplasia followed by an Open-Label Extension Period A Phase 2 study to evaluate the safety, efficacy and pharmacokinetics of TransCon CNP in prepubertal ... | ACcomplisH: A Phase 2, multicenter, double-blind, randomized, placebo-controlled, dose escalation trial evaluating safety, efficacy, and pharmacokinetics of subcutaneous doses of TransCon CNP administered once weekly for 52 weeks in prepubertal children with achondroplasia followed by an Open-Label Extension Period - ACcomplisH ACcomplisH: A Phase 2, multicenter, double-blind, randomized, placebo-controlled, dose escalation tr ... | Achondroplasia (ACH) in prepubertal children <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia;System Organ Class: 100000004850;Therapeutic area: Diseases [C] - Musculoskeletal Diseases [C05] Achondroplasia (ACH) in prepubertal children <br>MedDRA version: 20.0;Level: LLT;Classification code ... | Product Name: TransCon CNP 3.9 mg CNP-38/vial<br>Product Code: TransCon CNP<br>INN or Proposed INN: C-TYPE NATRIURETIC PEPTIDE CONJUGATED TO MULTI-ARM POLYETHYLENE GLYCOL CARRIER THROUGH A CLEAVABLE LINKER<br>Other descriptive name: C-TYPE NATRIURETIC PEPTIDE CONJUGATED TO MULTI-ARM POLYETHYLENE GLYCOL CARRIER THROUGH A CLEAVABLE LINKER Product Name: TransCon CNP 3.9 mg CNP-38/vial<br>Product Code: TransCon CNP<br>INN or Proposed INN: ... | Ascendis Pharma Growth Disorders A/S | NULL | Authorised-recruitment may be ongoing or finished | <an>br>Female: yes Male: yes | 60 | Phase 2 | United States;Portugal;Canada;Spain;Ireland;Denmark;Austria;Australia;Germany;United Kingdom;Switzerland;New Zealand United States;Portugal;Canada;Spain;Ireland;Denmark;Austria;Australia;Germany;United Kingdom;Switzer ... | ||
8 | EUCTR2020-001189-13-IT (EUCTR) | 05/02/2021 | 15/06/2021 | Phase 2 study of safety, tolerability, PK and efficacy of recifercept in achondroplasia | A PHASE 2 MULTIPLE DOSE, RANDOMIZED STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF RECIFERCEPT IN CHILDREN WITH ACHONDROPLASIA - - A PHASE 2 MULTIPLE DOSE, RANDOMIZED STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND E ... | Achondroplasia <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia;System Organ Class: 100000004850 <br>MedDRA version: 20.0;System Organ Class: 100000004850;Therapeutic area: Body processes [G] - Bones and nerves physological processes [G11] Achondroplasia <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia ... | Product Name: Recifercept<br>Product Code: [PF-07256472]<br>INN or Proposed INN: Recifercept | PFIZER INC | NULL | Authorised-recruitment may be ongoing or finished | <an>br>Female: yes Male: yes | 63 | Phase 2 | Portugal;United States;Spain;Belgium;Denmark;Australia;United Kingdom;Japan;Italy | ||
9 | EUCTR2020-001189-13-DK (EUCTR) | 22/12/2020 | 07/10/2020 | Phase 2 study of safety, tolerability, PK and efficacy of recifercept in achondroplasia | A PHASE 2 MULTIPLE DOSE, RANDOMIZED STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF RECIFERCEPT IN CHILDREN WITH ACHONDROPLASIA A PHASE 2 MULTIPLE DOSE, RANDOMIZED STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND ... | Achondroplasia <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia;System Organ Class: 100000004850;Therapeutic area: Body processes [G] - Bones and nerves physological processes [G11] Achondroplasia <br>MedDRA version: 20.0;Level: LLT;Classification code 10000452;Term: Achondroplasia ... | Product Name: Recifercept (proposed INN)<br>Product Code: PF-07256472<br>INN or Proposed INN: Recifercept (proposed INN)<br>Other descriptive name: TA-46 Product Name: Recifercept (proposed INN)<br>Product Code: PF-07256472<br>INN or Proposed INN: Recife ... | Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | NULL | Authorised-recruitment may be ongoing or finished | <an>br>Female: yes Male: yes | 63 | Phase 2 | Portugal;United States;Spain;Belgium;Australia;Denmark;Italy;Japan | ||
10 | NCT04638153 (ClinicalTrials.gov) | December 2, 2020 | 15/9/2020 | A Study Of Safety, Tolerability And Effectiveness Of Recifercept In Children With Achondroplasia | A PHASE 2 MULTIPLE DOSE, RANDOMIZED STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND EFFICACY OF RECIFERCEPT IN CHILDREN WITH ACHONDROPLASIA A PHASE 2 MULTIPLE DOSE, RANDOMIZED STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND E ... | Achondroplasia | Biological: Recifercept | Pfizer | NULL | Recruiting | 3 Months | 10 Years | All | 63 | Phase 2 | United States;Australia;Belgium;Denmark;Italy;Portugal;Spain |