Dfhcc.harvard.edu

Dfhcc.harvard.edu has Server used 155.52.219.206 IP Address with Hostname in United States. Below listing website ranking, Similar Webs, Backlinks. This domain was first Unknown and hosted in Boston United States, server ping response time 23 ms

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Hosting Provider

Website: Dfhcc.harvard.edu
Hostname: rcwp.dfci.harvard.edu
Country:
Region: MA
City: Boston
Postal Code: 02115
Latitude: 42.342399597168
Longitude: -71.087799072266
Area Code: 617
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Found 8 Websites with content related to this domain, It is result after search with search engine

Dana-Farber/Harvard Cancer Center Harvard T.H. Chan

Hsph.harvard.edu   DA: 20 PA: 7 MOZ Rank: 27

DF/HCC was formed in 1999 as a formal collaboration and is the powerful successor organization to the Dana-Farber Cancer Institute Comprehensive Cancer Center, one of the original cancer centers designated by the NCI in 1973.The cancer research and treatment collaborations sponsored across the participating institutions by the DF/HCC combines

DF/HCC IECD Application

Cure.dfhcc.harvard.edu   DA: 22 PA: 22 MOZ Rank: 45

  • The DF/HCC UMass Boston Summer Program to Advance Research Careers (SPARC) is a one-time, 12 WEEK program providing an intensive research experience focused on emerging technologies (ET) in cancer and cancer disparities
  • SPARC students will engage in full-time mentored cancer research experiences in research environments across DF/HCC and UMB

Umb-dfhcc.org

Umb-dfhcc.org   DA: 13 PA: 13 MOZ Rank: 28

  • The UMass Boston – DF/HCC Partnership is committed to developing a shared rigorous and collaborative transdisciplinary cancer and disparities-related research program
  • The UMass Boston – DF/HCC Partnership is committed to developing a shared rigorous and collaborative transdisciplinary cancer and disparities-related research program.

DF/HCC Clinical Trials

Clinicaltrials.dfhcc.harvard.edu   DA: 32 PA: 12 MOZ Rank: 47

This first-in-human open-label, multicenter, dose-escalation study is designed to evaluate the safety, tolerability, and PK of MTIG7192A alone or in combination with atezolizumab in participants with locally advanced, recurrent, or metastatic incurable tumors for whom standard therapy does not exist, has proven to be ineffective or intolerable, or is considered inappropriate, or for whom a

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