Canopus Biopharma (PK) (USOTC:CBIA)
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From Jan 2020 to Jan 2025
Canopus BioPharma, Inc. (OTCPK: CBIA), a biotechnology company
developing pharmaceutical products and assay methods for patients
suffering from infectious disease, radiation sickness, cancer, and
addiction, announced today that it will present at the Rodman & Renshaw
5th Annual Global Healthcare Conference in Monte Carlo, Monaco on
Monday, May 19, at 4:25 AM Eastern (10:25 AM Central European Summer
Time).
Patrick Prendergast, Chief Executive Officer of Canopus BioPharma, will
be presenting on behalf of the Company. Also in attendance will be Len
Rothstein, President, and Leo Prendergast, Chief Operating Officer. For
those unable to attend the event, the Canopus BioPharma presentation is
being webcast and can be accessed live or in replay format for a limited
time at the following link: http://www.wsw.com/webcast/rrshq13/cbia.pk.
Presentations by more than 175 emerging growth biotechnology companies
are expected Rodman & Renshaw 5th Annual Global Healthcare Conference
that rapidly has become the premier international event on the Life
Sciences calendar. Companies will share their accomplishments on an
array of therapeutic topics including oncology, cardiovascular disease,
central nervous system disorders, infectious diseases and medical device
technology. The event will unite companies with institutional investors,
venture capitalists, senior corporate executives and experts from the
scientific and medical communities. The Conference will include company
presentations, breakout sessions, and one-on-one meetings with
presenting companies.
About Rodman & Renshaw:
Rodman & Renshaw is a full-service investment bank dedicated to
providing investment banking services to companies that have significant
recurring capital needs due to their growth and development strategies.
We also provide research and sales and trading services to institutional
investor clients that focus on such companies. Since 2003, Rodman has
been a leading investment banking firm to the biotechnology sector, a
capital intensive market segment, as well as a leader in the PIPE
(private investment in public equity) and RD (registered direct
placements) transaction markets.
About Canopus BioPharma, Inc.:
Canopus BioPharma, Inc. (OTCBB: CBIA) is dedicated to providing the
safest, most cost effective and efficacious pharmaceutical products and
assay methods in the areas of infectious disease, radiation protection,
cancer, and addiction. With innovative science, proven research and
development leadership, and superior products and compounds, Canopus
BioPharma has, since 2001, been committed to becoming a market trend
setter in a new era of healthcare. In addition, the Company is a world
leader in the development of novel camelid antibody products to provide
unique avenues of progress and improvement in assay methods and
monitoring capabilities for physicians, patients and researchers,
initially for food chain protection applications. Canopus maintains
staff in Australia, South Africa, Ireland, Panama and the USA.
Additional information on the Company is available at www.canopusbiopharma.com.
Additional information on CB1400 is available from Canopus BioPharma
upon request from the contacts listed below on this press release.
With the exception of historical information contained in this press
release, content herein may contain “forward
looking statements” that are made pursuant to
the Safe Harbor Provisions of the Private Securities Litigation Reform
Act of 1995. These statements are based on management’s
current expectations and are subject to uncertainty and changes in
circumstances. In particular, the Company may not be successful in its
efforts commercialize or attain acceptable clinical results for its
products. Investors are cautioned that forward-looking statements
involve risks and uncertainties that could cause actual results to
differ materially from the statements made. These factors include
general economic conditions, delays and risks associated with the
performance of contracts and research and development programs,
uncertainties as a result of research and development, consumer and
industry acceptance, litigation and/or court proceedings, regulatory
risks including approval of Food and Drug Administration filings, the
ability to achieve and maintain revenues and profitability in the Company’s
business lines, and other factors discussed in the Company's filings
with the Securities and Exchange Commission.