Web Analytics

3 Latest Announced Rounds

  • $3,464,880
    Series A

    4 Investors

    Food and Beverage Retail
    Jan 14th, 2025
  • $300,000,000
    Series A

    2 Investors

    Biotechnology Research
    Jan 14th, 2025
  • $635,000
    Pre-Seed

    4 Investors

    Software Development
    Jan 14th, 2025
$2,188.81M Raised in 62 Funding Rounds in the past 7 Days - View All

Funding Round Profile

Normunity

start up
United States - ND
  • 14/01/2025
  • Series B
  • $75,000,000

Normunity, Inc., is a biotechnology company creating a new class of precision immuno-oncology medicines, called immune normalizers, that target novel mechanisms that free the body’s normal immunity against cancer. Based on an ongoing, interactive academic-biotech alliance with the lab of Dr. Lieping Chen at Yale School of Medicine, Normunity is targeting newly-discovered mechanisms of immune disruption in cancer based on proprietary discovery platforms that elucidate the complex interactions between human cancer and the immune system. The company is advancing an emerging pipeline of immune normalizers, including initial drug programs that target mechanisms that drive the exclusion of T-cells from immune-sensitive tumors and other mechanisms that are barriers to normal immune function in cancer. Normunity is located in Boston, Mass. and West Haven, Conn.


Related People

Rachel W. Humphrey, MDFounder

Rachel W. Humphrey, MD United States - Boston, Massachusetts

•Pharmaceutical executive with extensive experience in Product Development
from pre-IND to Phase IV/compound commercialization of small molecules, cytotoxics and biologics in oncology and immuno-oncology.

•Proven success in supervising Product Development strategy and tactics over ~18 years in 4 large pharmaceutical companies and in small biotech and with supervision of the successful development of 2 new molecular entities in oncology (NEXAVAR and YERVOY).

•As Senior Vice President and Head of Immuno-Oncology at AstraZeneca, successfully and swiftly (within 9 months) built a high-performing late-stage Immuno-Oncology department and supervised the initiation of the late stage global development of tremelimumab, MEDI4736 (PD-L1 inhibitor) and the treme/MEDI4736 combination.

•In the roles of Executive Vice President, Chief Medical Officer (Mirati Therapeutics, formerly MethylGene Inc.) and/or VP, Global Development (BMS) successfully managed all aspects of specific asset development including clinical, statistics, operations, regulatory, manufacturing, medical, publications, pre-launch and post-launch activities with a focus on global and regional development, including Asia and Japan.

•Extensive experience interacting internally with finance and research functions, and externally with investors, analysts, scientific leaders and large and small pharma collaborators.

•Extensive experience in-licensing compounds and interfacing, through Alliances, between large and small biotech companies.

•Broad interaction with global regulatory authorities including supervision of IND and NDA documents, ODAC preparation and label negotiations.

•Led improvement of process projects in global development and medical affairs.

•Participated on the leadership team and facilitated exit management following the BMS acquisition of Medarex and transition of Mirati Therapeutics from Canada to the US.