ID

44787

Description

Study ID: 110921 Clinical Study ID: 110921 Study Title: A Phase II Trial of Ofatumumab in Subjects with Waldenstrom's Macroglobulinemia Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00811733 Clinicaltrials.gov Link: https://clinicaltrials.gov/ct2/show/NCT00811733 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Ofatumumab Trade Name: N/A Study Indication: Waldenstrom Macroglobulinaemia The primary objective of this open-label, multi-center, Phase II study was to evaluate the safety and efficacy of Ofatumumab in subjects diagnosed with Waldenstrom Macroglobulinaemia. For the study, eligible subjects were enrolled to receive up to 3 cycles of treatment with Ofatumumab. The first cycle consisted of a single dose of 300 mg followed by 3 weekly doses of 1000 mg (Treatment Group A) or 4 weekly doses of 2000 mg (Treatment Group B) of Ofatumumab, with response assessment beginning at Week 12. Based on the Week 12-16 response, eligible subjects could receive up to 2 additional cycles of treatment. Depending on which items, this form has to be filled out at the Cycle 1 week 1, 2, 3 and 4 visits, Cycle 2 week 1, 2, 3 and 4 visits, Cycle 1 and 2 observation visits and unscheduled visits.

Lien

https://clinicaltrials.gov/ct2/show/NCT00811733

Mots-clés

  1. 26/11/2021 26/11/2021 - Sarah Riepenhausen
Détendeur de droits

GlaxoSmithKline

Téléchargé le

26 novembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 4.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733

PK Blood Sample

  1. StudyEvent: ODM
    1. PK Blood Sample
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
date of visit/assessment
Description

date of visit/assessment

Type de données

date

Alias
UMLS CUI [1]
C1320303
UMLS CUI [2]
C2985720
subject number
Description

subject ID

Type de données

text

Alias
UMLS CUI [1]
C2348585
visit type
Description

visit type

Type de données

text

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0332307
Dosing date and time
Description

Dosing date and time

Alias
UMLS CUI-1
C0178602
UMLS CUI-2
C1264639
Infusion start date/time
Description

[read-only]

Type de données

datetime

Alias
UMLS CUI [1,1]
C0574032
UMLS CUI [1,2]
C0439659
UMLS CUI [1,3]
C1264639
Infusion stop date/time
Description

[read-only]

Type de données

datetime

Alias
UMLS CUI [1,1]
C0574032
UMLS CUI [1,2]
C2746065
UMLS CUI [1,3]
C1264639
PK Blood Sample (Pre and Post Dose)
Description

PK Blood Sample (Pre and Post Dose)

Alias
UMLS CUI [1,1]
C0031328
UMLS CUI [1,2]
C0005834
Time relative to infusion
Description

For both cycles collect a sample for all timepoints herein in week 1 and 4, pre-infusion only in week 2 and 3. For the cycles' observation samples and "any time" samples this item is not needed.

Type de données

integer

Alias
UMLS CUI [1,1]
C0439564
UMLS CUI [1,2]
C3469597
UMLS CUI [1,3]
C0304229
UMLS CUI [1,4]
C0031328
UMLS CUI [1,5]
C0005834
Sample taken
Description

pharmacokinetics sample taken

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0031328
If yes, complete details, start date and actual start time
Description

Pre infusion, sample taken, start date/time

Type de données

datetime

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0031328
UMLS CUI [1,3]
C1264639
If yes, complete details, sample identifier
Description

Pre infusion, sample taken, sample identifier

Type de données

text

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0031328
UMLS CUI [1,3]
C1299222

Similar models

PK Blood Sample

  1. StudyEvent: ODM
    1. PK Blood Sample
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
date of visit/assessment
Item
date of visit/assessment
date
C1320303 (UMLS CUI [1])
C2985720 (UMLS CUI [2])
subject ID
Item
subject number
text
C2348585 (UMLS CUI [1])
Item
visit type
text
C0545082 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
visit type
CL Item
Cycle 1 week 1 (1)
CL Item
Cycle 1 week 2 (2)
CL Item
Cycle 1 week 3 (3)
CL Item
Cycle 1 week 4 (4)
CL Item
Cycle 1 Observation visit (5)
CL Item
Cycle 2 week 1 (6)
CL Item
Cycle 2 week 2 (7)
CL Item
Cycle 2 week 3 (8)
CL Item
Cycle 2 week 4 (9)
CL Item
Cycle 2 observation visit (10)
CL Item
unscheduled visit (11)
Item Group
Dosing date and time
C0178602 (UMLS CUI-1)
C1264639 (UMLS CUI-2)
Infusion start date/time
Item
Infusion start date/time
datetime
C0574032 (UMLS CUI [1,1])
C0439659 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
Infusion stop date/time
Item
Infusion stop date/time
datetime
C0574032 (UMLS CUI [1,1])
C2746065 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
Item Group
PK Blood Sample (Pre and Post Dose)
C0031328 (UMLS CUI [1,1])
C0005834 (UMLS CUI [1,2])
Item
Time relative to infusion
integer
C0439564 (UMLS CUI [1,1])
C3469597 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C0031328 (UMLS CUI [1,4])
C0005834 (UMLS CUI [1,5])
Code List
Time relative to infusion
CL Item
Pre-Infusion (1)
CL Item
End of infusion (2)
CL Item
1 hr post infusion (3)
pharmacokinetics sample taken
Item
Sample taken
boolean
C0005834 (UMLS CUI [1,1])
C0031328 (UMLS CUI [1,2])
Pre infusion, sample taken, start date/time
Item
If yes, complete details, start date and actual start time
datetime
C0005834 (UMLS CUI [1,1])
C0031328 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
Pre infusion, sample taken, sample identifier
Item
If yes, complete details, sample identifier
text
C0005834 (UMLS CUI [1,1])
C0031328 (UMLS CUI [1,2])
C1299222 (UMLS CUI [1,3])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial