BETHESDA, Md., April 16, 2015 /PRNewswire/ -- Northwest
Biotherapeutics, Inc. (NASDAQ: NWBO) ("NW Bio"), a
biotechnology company developing non-toxic DCVax® personalized
immune therapies for cancer, announced today that it has been
included in the Loncar Cancer Immunotherapy Index (LCINDX), a
professional index recently established to help investors better
track the immunotherapy field within the biotechnology
space.
The Index founders have selected "the top 25 companies" in the
immunotherapy space, including 6 big pharma companies and 19
growth-oriented biotech companies. The Index is designed to
capture the contributions of leading companies, both large and
small, to the progress of the immunotherapy field. The Index
currently ranks NW Bio 8th among the 25 companies
included.
The Index can be tracked on a daily basis at
http://www.loncarindex.com/
The Index is based upon the founders' view that "immunotherapy
is a transformational field within the biotechnology space" and
that "areas like immunotherapy trade on their own unique
circumstances and innovations."
"We welcome the advent of this new Index for the rapidly
advancing immunotherapy space," commented Linda Powers, CEO of NW Bio. "We
appreciate the Loncar Index' approach in assessing the companies
included, and we are pleased to see a recognition of NW Bio's
progress and position as a leader in the immunotherapy
space."
About Northwest Biotherapeutics
Northwest Biotherapeutics is a biotechnology company focused on
developing immunotherapy products to treat cancers more effectively
than current treatments, without toxicities of the kind associated
with chemotherapies, and on a cost-effective basis, in both
the United States and
Europe. The Company has a broad platform technology for DCVax
dendritic cell-based vaccines. The Company's lead program is
a 348-patient Phase III trial in newly diagnosed Glioblastoma
multiforme (GBM). GBM is the most aggressive and lethal form
of brain cancer, and is an "orphan disease." The Company is
under way with a 60-patient Phase I/II trial with DCVax-Direct for
all inoperable solid tumors cancers, with a primary efficacy
endpoint of tumor regression. It has completed enrollment in
the Phase I portion of the trial. The Company previously
received clearance from the FDA for a 612-patient Phase III trial
in prostate cancer. The Company conducted a Phase I/II trial
with DCVax for metastatic ovarian cancer together with the
University of Pennsylvania. In
Germany, the Company has received approval of a 5-year Hospital
Exemption for the treatment of all gliomas (brain cancer) patients
outside the clinical trial.
Disclaimer
Statements made in this news release that are not historical
facts, including statements concerning future treatment of patients
using DCVax and future clinical trials, are forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995. Words such as "expect," "believe,"
"intend," "design," "plan," "continue," "may," "will,"
"anticipate," and similar expressions are intended to identify
forward-looking statements. Actual results may differ
materially from those projected in any forward-looking
statement. Specifically, there are a number of important
factors that could cause actual results to differ materially from
those anticipated, such as risks related to the Company's ongoing
ability to raise additional capital, risks related to the Company's
ability to enroll patients in its clinical trials and complete the
trials on a timely basis, uncertainties about the clinical trials
process, uncertainties about the timely performance of third
parties, risks related to whether the Company's products will
demonstrate safety and efficacy, risks related to the Company's and
Cognate's abilities to carry out the intended manufacturing
expansions contemplated in the Cognate Agreements, risks related to
the Company's ability to carry out the Hospital Exemption program
and risks related to possible reimbursement and pricing.
Additional information on these and other factors, including Risk
Factors, which could affect the Company's results, is included in
its Securities and Exchange Commission ("SEC") filings.
Finally, there may be other factors not mentioned above or included
in the Company's SEC filings that may cause actual results to
differ materially from those projected in any forward-looking
statement. You should not place undue reliance on any
forward-looking statements. The Company assumes no obligation
to update any forward-looking statements as a result of new
information, future events or developments, except as required by
securities laws.
CONTACTS:
Les Goldman
202-841-7909
lgoldman@nwbio.com
Farrell Kramer (Media)
212-710-9685
Farrell.kramer@mbsvalue.com
Jane Searle (Investors)
212-710-9686
Jane.Searle@mbsvalue.com
www.nwbio.com
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SOURCE Northwest Biotherapeutics, Inc.