NCT02988817 · OUTCOME
Time of Maximum Plasma Concentration (Tmax) of Conjugated Enapotamab Vedotin for Dose-escalation Part
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEDIAN
- Unit
- Day
- Interval / dispersion
- Full Range
- Time frame
- For 1Q3W dosing regimen: Predose, EOI, and 2 and 5 hours after EOI on Day 1 of Cycles 1 and 3; For 3Q4W dosing regimen: Predose, EOI, and 2 and 5 hours after EOI on Day 15 of Cycles 1 and 3
What was measured
The Tmax of conjugated enapotamab vedotin for dose-escalation part is reported.
Analysis population: The PK analysis set included all participants who were exposed to at least 1 dose of enapotamab vedotin and who had at least 1 postdose PK measurement. 'Number analyzed' denotes the number of participants evaluated for the specified time point.
Groups in this outcome
Dose-escalation Part: Enapotamab Vedotin 0.3 mg/kg 1Q3W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 0.3 mg/kg 1Q3W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 1Q3W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 0.6 mg/kg 1Q3W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 1Q3W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 1.0 mg/kg 1Q3W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 1.5 mg/kg 1Q3W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 1.5 mg/kg 1Q3W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 2.0 mg/kg 1Q3W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 2.0 mg/kg 1Q3W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 2.2 mg/kg 1Q3W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 2.2 mg/kg 1Q3W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 2.4 mg/kg 1Q3W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 2.4 mg/kg 1Q3W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 3Q4W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 0.6 mg/kg 3Q4W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 0.8 mg/kg 3Q4W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 0.8 mg/kg 3Q4W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 3Q4W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 1.0 mg/kg 3Q4W until the end of treatment.
Dose-escalation Part: Enapotamab Vedotin 1.2 mg/kg 3Q4W
Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 1.2 mg/kg 3Q4W until the end of treatment.
| Group | Source count |
|---|---|
| Dose-escalation Part: Enapotamab Vedotin 0.3 mg/kg 1Q3W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 1Q3W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 1Q3W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 1.5 mg/kg 1Q3W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 2.0 mg/kg 1Q3W | 10 |
| Dose-escalation Part: Enapotamab Vedotin 2.2 mg/kg 1Q3W | 11 |
| Dose-escalation Part: Enapotamab Vedotin 2.4 mg/kg 1Q3W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 3Q4W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 0.8 mg/kg 3Q4W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 3Q4W | 6 |
| Dose-escalation Part: Enapotamab Vedotin 1.2 mg/kg 3Q4W | 3 |
Reported measurements
Cycle 1 Day 1
| Group | Source count |
|---|---|
| Dose-escalation Part: Enapotamab Vedotin 0.3 mg/kg 1Q3W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 1Q3W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 1Q3W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 1.5 mg/kg 1Q3W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 2.0 mg/kg 1Q3W | 10 |
| Dose-escalation Part: Enapotamab Vedotin 2.2 mg/kg 1Q3W | 10 |
| Dose-escalation Part: Enapotamab Vedotin 2.4 mg/kg 1Q3W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 3Q4W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 0.8 mg/kg 3Q4W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 3Q4W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 1.2 mg/kg 3Q4W | 0 |
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Dose-escalation Part: Enapotamab Vedotin 0.3 mg/kg 1Q3W | 0.06 | Not reported | 0.06 | 0.06 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 1Q3W | 0.03 | Not reported | 0.03 | 0.03 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 1Q3W | 0.036 | Not reported | 0.03 | 0.04 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 1.5 mg/kg 1Q3W | 0.033 | Not reported | 0.03 | 0.04 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 2.0 mg/kg 1Q3W | 0.032 | Not reported | 0.02 | 0.09 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 2.2 mg/kg 1Q3W | 0.032 | Not reported | 0.02 | 0.04 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 2.4 mg/kg 1Q3W | 0.03 | Not reported | 0.02 | 0.03 | Not reported |
Cycle 1 Day 15
| Group | Source count |
|---|---|
| Dose-escalation Part: Enapotamab Vedotin 0.3 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 1.5 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 2.0 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 2.2 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 2.4 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 3Q4W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 0.8 mg/kg 3Q4W | 3 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 3Q4W | 6 |
| Dose-escalation Part: Enapotamab Vedotin 1.2 mg/kg 3Q4W | 1 |
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 3Q4W | 14.010 | Not reported | 13.96 | 14.88 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 0.8 mg/kg 3Q4W | 14.058 | Not reported | 13.98 | 14.08 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 3Q4W | 14.083 | Not reported | 14.00 | 14.19 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 1.2 mg/kg 3Q4W | 13.98 | Not reported | 13.98 | 13.98 | Not reported |
Cycle 3 Day 1
| Group | Source count |
|---|---|
| Dose-escalation Part: Enapotamab Vedotin 0.3 mg/kg 1Q3W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 1Q3W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 1Q3W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 1.5 mg/kg 1Q3W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 2.0 mg/kg 1Q3W | 8 |
| Dose-escalation Part: Enapotamab Vedotin 2.2 mg/kg 1Q3W | 4 |
| Dose-escalation Part: Enapotamab Vedotin 2.4 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 3Q4W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 0.8 mg/kg 3Q4W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 3Q4W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 1.2 mg/kg 3Q4W | 0 |
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Dose-escalation Part: Enapotamab Vedotin 0.3 mg/kg 1Q3W | 0.04 | Not reported | 0.04 | 0.04 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 1Q3W | 0.03 | Not reported | 0.03 | 0.03 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 1Q3W | 0.04 | Not reported | 0.04 | 0.04 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 1.5 mg/kg 1Q3W | 0.030 | Not reported | 0.03 | 0.03 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 2.0 mg/kg 1Q3W | 0.036 | Not reported | 0.02 | 0.05 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 2.2 mg/kg 1Q3W | 0.042 | Not reported | 0.03 | 0.11 | Not reported |
Cycle 3 Day 15
| Group | Source count |
|---|---|
| Dose-escalation Part: Enapotamab Vedotin 0.3 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 1.5 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 2.0 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 2.2 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 2.4 mg/kg 1Q3W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 3Q4W | 0 |
| Dose-escalation Part: Enapotamab Vedotin 0.8 mg/kg 3Q4W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 3Q4W | 1 |
| Dose-escalation Part: Enapotamab Vedotin 1.2 mg/kg 3Q4W | 0 |
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Dose-escalation Part: Enapotamab Vedotin 0.8 mg/kg 3Q4W | 14.02 | Not reported | 14.02 | 14.02 | Not reported |
| Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 3Q4W | 13.98 | Not reported | 13.98 | 13.98 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 0.06
- upper Limit
- 0.06
- value
- 0.06
- group Id
- OG001
- lower Limit
- 0.03
- upper Limit
- 0.03
- value
- 0.03
- group Id
- OG002
- lower Limit
- 0.03
- upper Limit
- 0.04
- value
- 0.036
- group Id
- OG003
- lower Limit
- 0.03
- upper Limit
- 0.04
- value
- 0.033
- group Id
- OG004
- lower Limit
- 0.02
- upper Limit
- 0.09
- value
- 0.032
- group Id
- OG005
- lower Limit
- 0.02
- upper Limit
- 0.04
- value
- 0.032
- group Id
- OG006
- lower Limit
- 0.02
- upper Limit
- 0.03
- value
- 0.03
- denoms
- counts
- group Id
- OG000
- value
- 1
- group Id
- OG001
- value
- 1
- group Id
- OG002
- value
- 3
- group Id
- OG003
- value
- 3
- group Id
- OG004
- value
- 10
- group Id
- OG005
- value
- 10
- group Id
- OG006
- value
- 3
- group Id
- OG007
- value
- 0
- group Id
- OG008
- value
- 0
- group Id
- OG009
- value
- 0
- group Id
- OG010
- value
- 0
- units
- Participants
- title
- Cycle 1 Day 1
- categories
- measurements
- group Id
- OG007
- lower Limit
- 13.96
- upper Limit
- 14.88
- value
- 14.010
- group Id
- OG008
- lower Limit
- 13.98
- upper Limit
- 14.08
- value
- 14.058
- group Id
- OG009
- lower Limit
- 14.00
- upper Limit
- 14.19
- value
- 14.083
- group Id
- OG010
- lower Limit
- 13.98
- upper Limit
- 13.98
- value
- 13.98
- denoms
- counts
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 0
- group Id
- OG007
- value
- 3
- group Id
- OG008
- value
- 3
- group Id
- OG009
- value
- 6
- group Id
- OG010
- value
- 1
- units
- Participants
- title
- Cycle 1 Day 15
- categories
- measurements
- group Id
- OG000
- lower Limit
- 0.04
- upper Limit
- 0.04
- value
- 0.04
- group Id
- OG001
- lower Limit
- 0.03
- upper Limit
- 0.03
- value
- 0.03
- group Id
- OG002
- lower Limit
- 0.04
- upper Limit
- 0.04
- value
- 0.04
- group Id
- OG003
- lower Limit
- 0.03
- upper Limit
- 0.03
- value
- 0.030
- group Id
- OG004
- lower Limit
- 0.02
- upper Limit
- 0.05
- value
- 0.036
- group Id
- OG005
- lower Limit
- 0.03
- upper Limit
- 0.11
- value
- 0.042
- denoms
- counts
- group Id
- OG000
- value
- 1
- group Id
- OG001
- value
- 1
- group Id
- OG002
- value
- 1
- group Id
- OG003
- value
- 1
- group Id
- OG004
- value
- 8
- group Id
- OG005
- value
- 4
- group Id
- OG006
- value
- 0
- group Id
- OG007
- value
- 0
- group Id
- OG008
- value
- 0
- group Id
- OG009
- value
- 0
- group Id
- OG010
- value
- 0
- units
- Participants
- title
- Cycle 3 Day 1
- categories
- measurements
- group Id
- OG008
- lower Limit
- 14.02
- upper Limit
- 14.02
- value
- 14.02
- group Id
- OG009
- lower Limit
- 13.98
- upper Limit
- 13.98
- value
- 13.98
- denoms
- counts
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- group Id
- OG004
- value
- 0
- group Id
- OG005
- value
- 0
- group Id
- OG006
- value
- 0
- group Id
- OG007
- value
- 0
- group Id
- OG008
- value
- 1
- group Id
- OG009
- value
- 1
- group Id
- OG010
- value
- 0
- units
- Participants
- title
- Cycle 3 Day 15
- denoms
- counts
- group Id
- OG000
- value
- 1
- group Id
- OG001
- value
- 1
- group Id
- OG002
- value
- 3
- group Id
- OG003
- value
- 3
- group Id
- OG004
- value
- 10
- group Id
- OG005
- value
- 11
- group Id
- OG006
- value
- 3
- group Id
- OG007
- value
- 3
- group Id
- OG008
- value
- 3
- group Id
- OG009
- value
- 6
- group Id
- OG010
- value
- 3
- units
- Participants
- description
- The Tmax of conjugated enapotamab vedotin for dose-escalation part is reported.
- dispersion Type
- Full Range
- groups
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 0.3 mg/kg 1Q3W until the end of treatment.
- id
- OG000
- title
- Dose-escalation Part: Enapotamab Vedotin 0.3 mg/kg 1Q3W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 0.6 mg/kg 1Q3W until the end of treatment.
- id
- OG001
- title
- Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 1Q3W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 1.0 mg/kg 1Q3W until the end of treatment.
- id
- OG002
- title
- Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 1Q3W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 1.5 mg/kg 1Q3W until the end of treatment.
- id
- OG003
- title
- Dose-escalation Part: Enapotamab Vedotin 1.5 mg/kg 1Q3W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 2.0 mg/kg 1Q3W until the end of treatment.
- id
- OG004
- title
- Dose-escalation Part: Enapotamab Vedotin 2.0 mg/kg 1Q3W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 2.2 mg/kg 1Q3W until the end of treatment.
- id
- OG005
- title
- Dose-escalation Part: Enapotamab Vedotin 2.2 mg/kg 1Q3W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 2.4 mg/kg 1Q3W until the end of treatment.
- id
- OG006
- title
- Dose-escalation Part: Enapotamab Vedotin 2.4 mg/kg 1Q3W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 0.6 mg/kg 3Q4W until the end of treatment.
- id
- OG007
- title
- Dose-escalation Part: Enapotamab Vedotin 0.6 mg/kg 3Q4W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 0.8 mg/kg 3Q4W until the end of treatment.
- id
- OG008
- title
- Dose-escalation Part: Enapotamab Vedotin 0.8 mg/kg 3Q4W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 1.0 mg/kg 3Q4W until the end of treatment.
- id
- OG009
- title
- Dose-escalation Part: Enapotamab Vedotin 1.0 mg/kg 3Q4W
- description
- Participants with relapsed/refractory cancer (ovarian, cervical, endometrial, thyroid, NSCLC, or melanoma) received IV infusion of enapotamab vedotin 1.2 mg/kg 3Q4W until the end of treatment.
- id
- OG010
- title
- Dose-escalation Part: Enapotamab Vedotin 1.2 mg/kg 3Q4W
- param Type
- MEDIAN
- population Description
- The PK analysis set included all participants who were exposed to at least 1 dose of enapotamab vedotin and who had at least 1 postdose PK measurement. 'Number analyzed' denotes the number of participants evaluated for the specified time point.
- reporting Status
- POSTED
- time Frame
- For 1Q3W dosing regimen: Predose, EOI, and 2 and 5 hours after EOI on Day 1 of Cycles 1 and 3; For 3Q4W dosing regimen: Predose, EOI, and 2 and 5 hours after EOI on Day 15 of Cycles 1 and 3
- title
- Time of Maximum Plasma Concentration (Tmax) of Conjugated Enapotamab Vedotin for Dose-escalation Part
- type
- SECONDARY
- unit Of Measure
- Day
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Preserved source evidence · Not medical advice
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