Scheduling, administration, biomarkers, and practical guidance.
Standard-sensitivity protocol; prevents tachyphylaxis and limits cumulative pro-angiogenic exposure.
Phase 2 trial duration is a reasonable upper bound for continuous dosing.
Maintenance paradigm; not yet established whether off-cycles are needed in cardiovascular use.
Manufacturer-recommended pulse protocol; human clinical data limited.
Not daily — longer half-life supports intermittent dosing.
Standard practice to maintain receptor sensitivity.