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Dosing & administration

Starting dose

BLENREP + Vd: Individualized dosing protocol

This treatment regimen involves the administration of BLENREP in combination with bortezomib and dexamethasone (BVd). BLENREP should be administered until disease progression or unacceptable toxicity.

Recommended starting dose schedule for BLENREP in the BVd triplet combination

CYCLES 1-8 CYCLE 9+

BLENREP + Vd

2.5 mg/kg once every 3 weeks

BLENREP monotherapy

2.5 mg/kg once every 3 weeks

until treatment completion

Cycle length = 3 weeks

Adapted from the Product Monograph.

BLENREP + Pd: Individualized dosing protocol

This treatment regimen involves the administration of BLENREP in combination with pomalidomide and dexamethasone (BPd). BLENREP should be administered until disease progression or unacceptable toxicity.

Recommended starting dose schedule for BLENREP in the BPd triplet combination

CYCLE 1 CYCLE 2+

BLENREP + Pd

2.5 mg/kg once

BLENREP + Pd

1.9 mg/kg once every 4 weeks

until treatment completion

Cycle length = 4 weeks

Adapted from the Product Monograph.

Dose modifications

BLENREP dose modifications for eye-related side effects in combination with Vd

BLENREP dose modification flowchart for eye-related side effects in combination with Vd.
Adapted from the Product Monograph.
  • Refer to the respective Product Monographs of medications used in the BVd combination for complete information on dosing and administration.

*Ocular adverse reaction severity is defined by the most severely affected eye as both eyes may not be affected to the same degree.

BVd: BLENREP + bortezomib and dexamethasone; ERSE: Eye-related side effects; Q3W: Every three weeks; AR: Adverse reaction.

Dose modifications, including delays and reductions, were frequently required to manage adverse reactions, including eye-related side effects

  • Among patients who experienced an eye-related side effect, 91% (n=190/209) continued treatment on or after the onset of the first event and received a median of 8 additional doses (range: 1 to 52)
  • Permanent discontinuation of any component of BVd due to eye-related side effects, including ocular adverse reactions, visual acuity changes, or corneal examination findings, occurred in 10% of patients
DREAMM-7 table of observed dose delays and reductions for BLENREP + Vd.
Adapted from the Product Monograph.

*DREAMM-7 was conducted in patients with multiple myeloma who have received at least one prior therapy. These patients were randomized in a 1:1 ratio to receive either BVd (n=243) or DVd (n=251).

†Intervals for 0 to ≤6 months, >6 to ≤12 months, and >12 months were calculated either by using days or days converted into months.

IQR: Interquartile range.

BLENREP dose modifications for eye-related side effects in combination with Pd

BLENREP dose modification flowchart for eye-related side effects in combination with Pd.
Adapted from the Product Monograph.
  • Refer to the respective Product Monographs of medications used in the BPd combination for complete information on dosing and administration.

*Pomalidomide and dexamethasone may be continued during BLENREP dose holds, if warranted, per the judgement of the treating physician.

†Ocular adverse reaction severity is defined by the most severely affected eye as both eyes may not be affected to the same degree.

‡If toxicity is identified prior to dosing cycle 2 for BPd, dose at 1.9 mg/kg every 4 weeks.

BPd: BLENREP + pomalidomide and dexamethasone; AR: Adverse reaction; ERSE: Eye-related side effects; Q4W: Every four weeks; Q8W: Every eight weeks.

Dose modifications, including delays and reductions, were frequently required to manage adverse reactions, including eye-related side effects

  • Among patients who experienced an eye-related side effect, 92% (n=120/131) continued treatment on or after the onset of the first event and received a median of 5 additional doses (range: 1 to 21)
  • Permanent discontinuation of any component of BPd due to eye-related side effects, including ocular adverse reactions, visual acuity changes, or corneal examination findings, occurred in 11% of patients
DREAMM-8 table of observed dose delays and reductions for BLENREP + Pd.
Adapted from the Product Monograph.

*DREAMM-8 was conducted in patients with multiple myeloma who have received at least one prior therapy, including lenalidomide. These patients were randomized in a 1:1 ratio to receive either BPd (n=155) or PVd (n=147).

†Intervals for 0 to ≤6 months, >6 to ≤12 months, and >12 months were calculated either by using days or days converted into months.

IQR: Interquartile range.

Administration

Preparation

Detailed guidance to be added once the BLENREP Dosing & Administration Guide content is finalized. In the meantime, refer to the Product Monograph.

Infusion guidelines

Detailed guidance to be added once the BLENREP Dosing & Administration Guide content is finalized. In the meantime, refer to the Product Monograph.

Pre-medication

Detailed guidance to be added once the BLENREP Dosing & Administration Guide content is finalized. In the meantime, refer to the Product Monograph.

Patient monitoring during and after infusion

Detailed guidance to be added once the BLENREP Dosing & Administration Guide content is finalized. In the meantime, refer to the Product Monograph.

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References

  1. BLENREP Product Monograph. GSK, [Date placeholder].
  2. Hungria V, et al. N Engl J Med. 2025;392(13):1213–1224. (DREAMM-7)
  3. Trudel S, et al. N Engl J Med. 2025;393(2):166–178. (DREAMM-8)