Protagonist Therapeutics reported its second quarter financial results, highlighting the advancement of three differentiated candidates into Phase 2 development and a successful secondary offering and ATM program, ensuring financial resources to support operations through mid-2023.
Three differentiated candidates advanced from de novo discovery into Phase 2 development.
PTG-300 received U.S. Food and Drug Administration (FDA) Orphan Drug Designation for the treatment of polycythemia vera.
Expect to initiate a pivotal study for PTG-300 in 2021 after discussions with the regulatory agencies.
Financial resources expected to support operations through mid-2023.
Protagonist Therapeutics anticipates continued progress in its clinical programs and expects financial resources to support operations through mid-2023.