EX-99.1 2 d816002dex991.htm EX-99.1 EX-99.1

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AVEO Overview November 2019


Slide 2

Cautionary Note Regarding Forward-Looking Statements


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Slide 4

Multiple Potential Opportunities for Value Creation


Slide 5

Financial Highlights


Slide 6

FOTIVDA® (tivozanib) TIVO-3 Pivotal Phase 3 Study


Slide 7

Tivozanib: VEGFR 1, 2 and 3 Tyrosine Kinase Inhibitor


Slide 8

TIVO-3: Study Design


Slide 9

TIVO-3: Superior PFS and ORR*


Slide 10

Progression-Free Survival – Key Subgroups*


Slide 11

Durable Disease Control with Tivozanib (Patients with > 1 year PFS)


Slide 12

Secondary Endpoint – Overall Survival


Slide 13

Pre-NDA Regulatory Feedback and POA


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As OS Data Matures HR Improves


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Treatment-Related Adverse Events* (≥20% frequency in either arm)


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Slide 17

TIVO-3 Conclusions


Slide 18

PD-1 Combination Opportunities


Slide 19

Tivozanib Properties May Provide Advantages in Combination with IO Therapy


Slide 20

Phase 2 Data Presented at ESMO in September 2019


Slide 21

ESMO 2019: Encouraging Safety Results


Slide 22

ESMO 2019: Encouraging Efficacy


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Combination of PD-1 + VEGF TKIs: Promising Responses, All Phase 3 Currently 1st Line


Slide 24

TiNivo – Strong Efficacy Seen in Both Treatment Naive and Previously Treated Patients


Slide 25

Immuno-Oncology Clinical Collaboration with AstraZeneca


Slide 26

Tivozanib Commercial Opportunity


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If Approved, Significant Potential Commercial Opportunity for Tivozanib in the United States


Slide 28

Potential Relevance of Tivozanib in Refractory RCC


Slide 29

FOTIVDA® Commercialization in EU and ROW


Slide 30

Pipeline and Near-Term Milestones


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Slide 35

AVEO Key Near Term Potential Milestones


Slide 36

AVEO Overview November 2019