Hana Biosciences recovering from recent price drop Print E-mail
By Eric Sebastien   
Wednesday, 17 November 2010 03:21

penny stock picksHana Biosciences, Inc. (OTC:HNAB) has been busy getting ready to submit- in first half of 2011- a complete original NDA. 


"During the third quarter of 2010, our focus was on preparation of the 5 modules that make up the NDA submission for Marqibo" stated Dr. Steven R. Deitcher, M.D., President and Chief Executive Officer of Hana Biosciences during a recent conference call. "An analysis of data from the Menadione Topical Lotion Phase 1 program showed that it was generally safe and well tolerated. In addition, the dose limiting toxicity and apparent maximum tolerated lotion strength were identified. Our strategy is to seek a partner to enhance and accelerate the continued development of Menadione Topical Lotion.

While some investors considered this positive news, others simply took their profits off the table after the recent rise in share prices (+50% in one month) and wlaked away.  HNAB was suddenly down 28% on low volume. Now some are re-considering HNAB and its potential as a "good buy opportunity", especially since the complete submission of the NDA is just months away.

Hana Biosciences was working on preparing the 5 modules during the third quarter and this will carry on through the end of the year, almost all of the modules will be completed before the end of 2010, we believe a change for a full submission rather than module by module might be a good strategy and Dr. Deitcher mentioned during the CC that it was suggested and recommended by the FDA, it is most convenient for them.

As of September 30, 2010, the Company had cash, cash equivalents and available-for-sale securities of $27.7 million. With the recent $40M financing round, that brings the market cap of Hana Biosciences to around $50M, which we consider to be still very low regarding the pipeline, and the long term potential for Marqibo in other indications.

I recenlty conducted an exclusive interview with Hana Biosciences:

Question:  You are about to fill the rolling NDA for Marqibo, are you confident to get an accelerated approval review? You said the NDA will be filled before end of 2010, are you still on track with this time frame?

Craig Carlson, CFO of Hana Biosciences: 
On November 8, 2010 we held a pre-NDA follow-up meeting with the FDA. At that meeting we and the FDA agreed that Hana would submit all of the NDA modules simultaneously instead of following a rolling submission process. This change in process is not expected to effect the timing of submission completion, review or potential approval. We anticipate submitting the completed NDA in the first half of 2011. We are pursuing an accelerated approval of Marqibo and the program already has Fast-Track and Orphan Drug designations from the FDA.

HNAB Investors Reevaluate the Stock

Question: Can you confirm that other applications with Marqibo such as Front-line NHL and Front-line Ph-ALL which represent a total market of around 5B will both only require Phase III studies? Are they already started or when do you plan to start them?


Craig Carlson, CFO of Hana Biosciences:
  We expect that studies such as the ones you indicated will only require Phase III studies. However, until a Phase III trial protocol is approved by the FDA there is not 100% certainty. No Phase III clinical trials of Marqibo have commenced. The logical strategy is to receive the FDA’s approval decision on Marqibo’s current indication before committing funds to a large, expensive, label expansion trial.

Question: Are those other applications with Marqibo already founded or do you plan to partner with the classic method of upfront payment and royalties system?

Craig Carlson, CFO of Hana Biosciences:  For large, expensive, multi-national, Phase III clinical trials, it is common for small companies to seek to share costs with another entity. We are keeping all our options open.
 
Question: Marqibo has been granted EMA Orphan Drug designation in Europe and you said you are exploring the potential for an authorization under exceptional circumstances. Can you tell us more about this process and does it mean Marqibo may be approved in Europe in 1H11?

Craig Carlson, CFO of Hana Biosciences:  Hana will seek formal Scientific Advice from EMA in 2011. Approval in Europe will require a full regulatory submission.  The approval decision in Europe is anticipated to follow the approval decision in the US.

Question: There is actually one clinical trial that is ongoing with the NCI with respect to pediatric cancers ALL, when will we have some data about this promising indication?

Craig Carlson, CFO of Hana Biosciences:  The pediatric oncology branch of the NCI will be conducting a Phase 1 pharmacokinetic and dose finding study. The study could take up to 2 years to fully enroll.

Question: Now, with respect to Menadione, we are waiting for Top-line data and the start of the Phase II before end of this year. The focus is on Marqibo for now and investors have yet to discover the potential of this topical cream. Since it has the potential to prevent the rash in chemotherapy treated patients and it is also effective to treat psoriasis, can you tell enlighten us about the market potential in term of numbers?

Craig Carlson, CFO of Hana Biosciences:  First, we have no clinical data demonstrating the efficacy of Menadione Topical Lotion for treating psoriasis. We recently completed the Phase 1 program.  The Phase 1 program has successfully demonstrated that MTL is generally safe and well-tolerated.  The dose limiting toxicity, skin irritation and redness, was only observed at the 0.2% lotion strength.  The apparent maximum tolerated lotion strength is 0.1%.   MTL applied twice daily at all strengths, including the highest lotion strength tested (0.2%) resulted in no appreciable systemic exposure.

Due to the fact that there are no comparable lotions indicated for the treatment of EGFR rash, there is no empirical data establishing the size of the opportunity.  It is estimated that there are approximately 45,000 to 50,000 people undergoing EGFR therapy annually in the U.S and Europe.

Question: Since Menadione is a topical cream, does it need to go through a classic FDA review process with a NDA filing? You said you plan to find a partner for Menadione, you mentioned discussions with partners are ongoing, can you tell us more about this?

Craig Carlson, CFO of Hana Biosciences:  Menadione Topical Lotion requires the completion of the standard FDA clinical trial process. We are unable to comment on discussions with potential partners.

Question: You recently signed a financing deal with Warburg Pincus for up to $100M. While many investors fear dilution to come, can you explain the Warburg’s strategy with your company? Do you feel it’s a long term partner that will push Hana Bioscience to a bigger company?


Craig Carlson, CFO of Hana Biosciences:  Warburg Pincus has a track record as a long-term investor seeking to generate significant value but we are unable to predict how things will progress with Hana at this time.

Question: There has been some misunderstanding with the convert prices post R/S. Can you confirm that convert prices did increase 4X also with the R/S and are now at $0.72 and $1.10? We have seen that Warburg is a long term partner with companies they invest on, do you think they will convert and sell their shares on the market or rather they will wait to get the full potential in the coming years before selling any?

Craig Carlson, CFO of Hana Biosciences:  The new conversion prices are $0.736 for the Series A-1 Preferred Stock and $1.104 for the Series A-2 Preferred Stock. Based on the Investment Agreement, the preferred shareholders have options for how they may choose to create liquidity for their preferred shares, including converting to common shares or, if there is an acquisition, preferred shareholders may opt to receive proceeds in cash without converting into common shares. We are unable to predict if or when preferred shareholders may choose to convert their preferred shares to common shares.

Question: We know that Warburg has a large portfolio of biotech companies that are almost all traded on the NASDAQ with a market cap of over $500M, do you think we might see HNAB back to the NASDAQ in early 2011?


Craig Carlson, CFO of Hana Biosciences:
There are certain requirements to be listed on exchanges such as Nasdaq and Amex. Among the requirements are share price, stock holder equity, and market cap, as well as others. We are unable to predict when Hana may meet the necessary requirements, if at all.

Writer Eric Sebastien is the managing editor of TheCleverBull.com
Disclosure: Long HNAB



"Featured Content" profiles are meant to provide awareness of these companies to investors in the small-cap and growth equity community and should not in any way come across as a recommendation to buy, sell or hold these securities. BiomedReports is not paid or compensated by newswires to disseminate or report news and developments about publicly traded companies, but may from time to time receive compensation for advertising, data, analytics and investor relation services from various entities and firms. Full disclosures should be read in the 'About Us Section'.

Add this page to your favorite Social Bookmarking websites
Digg! Reddit! Del.icio.us! Mixx! Google! Live! Facebook! Technorati! StumbleUpon! MySpace! Yahoo!

blog comments powered by Disqus
 

Newsletter