SBIR/STTR Research Award
M40403 and IL-2 Induced Hypotension
Award amount
$104,000Program and phase
SBIR · Phase IAward year
2001Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- METAPHORE PHARMACEUTICALS, INC.
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
DESCRIPTION (provided by applicant): The lymphokine interleukin 2 (IL-2) is
currently approved by the FDA as therapy for metastatic renal cell carcinoma
and malignant melanoma. The clinical use of IL-2 has been limited by its severe
side effects, particularly hypotension. Because of such dose-limiting side
effects, the full period of IL-2 dosing is frequently curtailed. We have found
that M40403, MetaPhores prototypic superoxide dismutase mimetic (SODm)
completely attenuated IL-2 induced hypotension & allowed the dose of IL-2 to be
escalated from 180,000IU to 400,000IU. M40403 did not interfere with the
anti-tumor effects of IL-2. In contrast, M40403 increased IL-2 mediated
activation of the lymphokine activated killer cells as demonstrated by in vitro
& in vivo experiments & synergized with the anti-tumor effects of IL-2 in in
vivo tumor models. These preliminary results suggest that M40403 inhibits the
dose limiting toxicity of IL-2 administration without interfering with its
antitumor effects. In fact, our data suggests a potentiation of the anti-tumor
effects of IL-2. Thus, clinical evaluation of M40403 is warranted because 1) it
reverses IL-2 induced hypotension 2) it increases IL-2 induced anti-cancer
responses & 3) it has a direct anti-cancer activity. Based on preliminary data
summarized above, MetaPhore's goals are to complete the preclinical evaluation
of M40403 & to test the capacity of this agent to attenuate the dose limiting
toxicity (hypotension) of IL-2 in a clinical trial. If the preliminary data is
confirmed by the work proposed in this Phase I application, we would expect to
follow aggressively into a Phase II development effort to move this drug
candidate forward to clinical trials.
PROPOSED COMMERCIAL APPLICATION: NOT AVAILABLE
Technology keywords
Not reported