
Dekk-Tec Inc Profile last edited on: 6/12/18
CAGE: 476W4
UEI: E9MHC27T2XK3
Business Identifier: Anti-cancer agents able to cross the blood brain barrier Is this YOUR Company?
Ensure accuracy and completeness of YOUR Company Profile by completing the brief Survey Instrument attached
Do you know about this Awardees?
Let us encourage you to provide any data which would enhance the completeness of this firm's profile.
Location Information
Location: Single
Congr. District: 01
County: Orleans Parish
Congr. District: 01
County: Orleans Parish
Public Profile
Dekk-Tec Inc is developing new therapies and clinical candidates for the management of cancer, allied diseases, pre-cancerous lesions and women's health issues. The firm is evaluating a novel phenylhydrazone as an immune modulator for treating anogenital cancer associated with human papilloma virus infection. DM-CHOC-PEN, the firmâs lead proprietary investigational anticancer agent, is able to be administered intravenously, cross the blood brain barrier and localize in cancer tissue. Many cancer drugs are not able to cross this barrier and thus must be given intra-cranially, which can cause significant toxicity with only modest efficacy. Dekk-Tec's product has favorable safety, toxicity and PK/PD profiles with superior efficacy to available therapies in pre-clinical studies. As such, DM-CHOC-PEN represents a significant new cancer therapy opportunity to address a large unmet medical need. Dekk-Tec has previously licensed two of their pipeline products to Biotech/Pharmaceutical companies
Extent of SBIR involvement
Synopsis: Awardee Business Condition
Employee Range
5-9Revenue Range
.5M-1MVC funded?
NoPublic/Private
Privately HeldStock Info
----IP Holdings
5-9Awards Distribution by Agency
Most Recent SBIR Projects
Year | Phase | Agency | Total Amount | |
---|---|---|---|---|
2020 | 2 | NIH | $1,441,954 | |
Project Title: Phase I Clinical Trial with 4-Demethyl-4-Cholesteryloxycarbonylpenclomedine (DM-CHOC-PEN) in Children with Cancer Involving the Cns | ||||
2018 | 2 | NIH | $286,588 | |
Project Title: A Phase I Clinical Trial: Binary Therapy withDM-CHOC-PEN and Wbrt in Adults with Cancer Involving the CNS | ||||
2014 | 2 | NIH | $1,434,110 | |
Project Title: 4-Demethyl-4-Cholesteryloxycarbonylpenclomedine (Dm-Choc-Pen): A Phase I Clinial | ||||
2011 | 2 | NIH | $996,112 | |
Project Title: Camptothecin Analogs for Cancer Therapy | ||||
2007 | 2 | NIH | $724,765 | |
Project Title: Clinical Development of 4-Hydroperoxyifosfamide |
Key People / Management
Lee Roy Morgan -- Chief Executive Officer, Director of Research
Lee Roy Morgan
Andrew H Rodgers -- Director of Regulatory Affairs
Lee Roy Morgan
Andrew H Rodgers -- Director of Regulatory Affairs
Company News
There are no news available.