“Group effect” in BE [Surveys]
Dear all,
I created an open survey to gather information about the current (and past) state of affairs. Ten questions, less than five minutes to answer. Feel free to join.
Sneak preview (what to expect) below:
Multigroup studies
Design
How do you design a multigroup study?
Pooling of data
Procedures (1/2)
Do you routinely pool data?
Pooling of data
Procedures (2/2)
Do you justify in the protocol why you consider pooling of data a valid approach?My interpretation of the EMA’s BE guideline
It is a source of variation that cannot be reasonably assumed to have an effect on the response variable.
Other
Please specify.
Models
Procedures
Do you assess models recommended by the FDA?
Models
Observations (please skip if you didn’t assess model 1)
How often did you observe a significant Group-by-Treatment interaction?
Applicability
Regulatory acceptance (protocol)
Was your approach accepted?
Applicability
Regulatory acceptance (report)
Was your approach accepted?
Problems
Deficiency letters, rejected studies, etc.
In which country / jurisdiction / with which agency did you face the most problems?
I created an open survey to gather information about the current (and past) state of affairs. Ten questions, less than five minutes to answer. Feel free to join.
Sneak preview (what to expect) below:
Multigroup studies
Design
How do you design a multigroup study?
- Staggered
(i.e., immediately after one group has finished a period, the next group starts theirs)
- Stacked
(i.e., complete all periods of one group before the next group starts)
- Both
(case by case, e.g., staggered for single dose studies and stacked for multiple dose studies)
Pooling of data
Procedures (1/2)
Do you routinely pool data?
- Yes
I don’t take multigroup nature of study into account.
- Yes
But I adjust the statistical model accordingly.
- Case by case
I follow a decision scheme.
Pooling of data
Procedures (2/2)
Do you justify in the protocol why you consider pooling of data a valid approach?
- Always
- Never
- Case by case
Please give an example.
- Based on the FDA’s
- The clinical study takes place at one site,
- all study subjects have been recruited from the same enrollment pool,
- all of the subjects have similar demographics, and
- all enrolled subjects are randomly assigned to treatment groups at study outset.
It is a source of variation that cannot be reasonably assumed to have an effect on the response variable.
Please specify.
Models
Procedures
Do you assess models recommended by the FDA?
- Group, Sequence, Treatment, Subject (nested within Group × Sequence), Period (nested within Group), Group-by-Sequence Interaction, Group-by-Treatment Interaction.
- Group, Sequence, Treatment, Subject (nested within Group × Sequence), Period (nested within Group), Group-by-Sequence Interaction.
- Sequence, Treatment, Period, Subject (nested within Sequence).
- Yes
- No
- Don’t know
- If the G×T term in model 1 is ≥0.1, assess BE by model 2 of pooled data.
- If the G×T term in model 1 is <0.1, assess BE by model 3 of the groups.
- Yes
- No
I pool data and use model 2 without a pre-test.
- No
I pool data and use model 3 (as if it is a single group study).
- Don’t know
Models
Observations (please skip if you didn’t assess model 1)
How often did you observe a significant Group-by-Treatment interaction?
- In much less than 10% of studies
- In about 10% of studies
- In much more than 10% of studies
- Don’t know
- Other
If possible, give the number of studies with a significant G×T term and the total number of studies.
Example: 7 / 65.
Applicability
Regulatory acceptance (protocol)
Was your approach accepted?
- Yes
Justification for not assessing the G×T. Pooling of data and evaluation by model 3 planned.
- Yes
Following the decision scheme planned; dependent on the G×T by model 1:
p ≥0.1: Pooled data by model 2.
p <0.1: Data of the largest group by model 3.
- Yes
Pooled data by model 2 (without the pre-test) planned.
- Yes
Pooled data by model 3 planned but nothing specifically stated.
- No
(please give the reason for the rejection of your approach and – if possible – the agency and year).
Applicability
Regulatory acceptance (report)
Was your approach accepted?
- Yes
Justification for not assessing the G×T given in the SAP.
Evaluation of pooled data by model 3.
- Yes
The decision scheme observed.
Evaluation of pooled data by model 2 or model 3 of the largest group.
- Yes
Evaluation of pooled data by model 2 (without a pre-test) performed.
- Yes
I didn’t take the multigroup nature of study into account.
Evaluation of pooled data by model 3.
- No
(please give the reason for the rejection of your evaluation and – if possible – the agency and year).
Problems
Deficiency letters, rejected studies, etc.
In which country / jurisdiction / with which agency did you face the most problems?
- USA
- MENA States
- Russian Federation
- Eurasian Economic Union (except Russia)
- European Economic Area (EU; Iceland, Liechtenstein. Norway)
- Brazil
- ASEAN States
- Other
(please give the reason for the rejection of your evaluation and – if possible – the agency and year).
Alternatively: Agency and year where you faced no problems.
—
Dif-tor heh smusma 🖖🏼 Довге життя Україна!
Helmut Schütz
The quality of responses received is directly proportional to the quality of the question asked. 🚮
Science Quotes
Dif-tor heh smusma 🖖🏼 Довге життя Україна!
Helmut Schütz
The quality of responses received is directly proportional to the quality of the question asked. 🚮
Science Quotes
Complete thread:
- “Group effect” in BEHelmut 2017-05-27 14:07
- “Group effect” in BE Ben 2017-05-31 20:02
- “Group effect” in BE Helmut 2017-05-31 20:38
- “Group effect” in BE Ben 2017-06-05 17:25
- “Group effect” in BE Helmut 2017-05-31 20:38
- “Group effect” in BE Ben 2017-05-31 20:02