Rollover Study for Subjects Who Have Participated in an Astellas Sponsored ASP2215 Trial

Inclusion Criteria:

- Subject must currently be participating in an Astellas sponsored, single agent ASP2215
trial, receiving ASP2215 and have not met any discontinuation criteria of the parent
study and can enroll into this rollover study without interruption of study drug, or
with no more than 2 weeks interruption in study drug.

- Subject must be deriving benefit from continued treatment without any persistent
intolerable toxicity from continued treatment of ASP2215.

- Female subject must either:

- Be of non-childbearing potential: post-menopausal (defined as at least 1 year
without any menses) prior to Screening, or documented surgically sterile or
post-hysterectomy (at least 1 month prior to Screening)

- Or, if of childbearing potential, Agree not to try to become pregnant during the
study and for 180 days after the final study drug administration; And have a
negative urine pregnancy test at Day 1; And, if heterosexually active, agree to
consistently use two forms of highly effective birth control (at least one of
which must be a barrier method) starting at Screening and throughout the study
period and for 180 days after the final study drug administration.

- Female subject must agree not to breastfeed starting at Screening and throughout the
study period, and for 60 days after the final study drug administration.

- Female subject must not donate ova starting at Screening and throughout the study
period, and for 180 days after the final study drug administration.

- Male subject and their female spouse/partners who are of childbearing potential must
be using highly effective contraception consisting of two forms of birth control (at
least one of which must be a barrier method) starting at Screening and continue
throughout the study period, and for 120 days after the final study drug
administration.

- Male subject must not donate sperm starting at Screening and throughout the study
period and, for 120 days after the final study drug administration.

- Subject agrees not to participate in another interventional study while on treatment.

Exclusion Criteria:

- Subject requires treatment with concomitant drugs that are strong inducers of
cytochrome P450 (CYP)3A.

- Subject requires treatment with concomitant drugs that target serotonin
5-hydroxytryptamine receptor 1 (5HT1R) or 5-hydroxytryptamine receptor 2B (5HT2BR) or
sigma nonspecific receptor with the exception of drugs that are considered absolutely
essential for the care of the subject.

- Subject requires treatment with concomitant drugs that are strong inhibitors or
inducers of P-glycoprotein (P-gp) with the exception of drugs that are considered
absolutely essential for the care of the subject.