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SEC Comment Letter for Traws Pharma, Inc. (TRAW) (CIK 0001130598) (TRAW) — Jun 28, 2013

Traws Pharma, Inc. (TRAW) (CIK 0001130598)
Date: June 28, 2013 · CIK: 0001130598 · Accession: 0000000000-13-035535

AI Filing Summary & Sentiment

Sentiment
Urgency
Document Type
Confidence
SEC Posture
Company Posture

Summary

Reasoning

Date
June 14, 2013
Author
/s/ Jeffrey P. Riedler
Form
UPLOAD
Company
Traws Pharma, Inc. (TRAW) (CIK 0001130598)

Letter

June 28 , 2013 Via E -mail Ramesh Kumar, Ph.D. President and Chief Executive Officer Onconova Therapeutics, Inc. 375 Pheasant Run Newtown, PA 18940

Re: Onconova Therapeutics, Inc. Registration Statement on Form S -1 Filed June 14 , 2013 File No. 333 -189358

Dear Dr. Kumar:

We have r eviewed your registration statement filed June 14, 2013 and your response to our comments to your confidential draft registration statement submitted on May 3, 2013 and have the following comments. In some of our comments, we may ask you to provide us with infor mation so we may better understand your disclosure.

Please respond to this letter by providing the requested infor mation and amending your registr ation statement . If you do not believe our comments apply to your facts and circu mstances or do not believe an amendment is a ppropriate, please tell us why in your response.

After revie wing the infor mation you provide in response to these com ments, we may have additio nal co mments.

Management’s Discussion and Analysis, page 55 Financial Overview, page 58

1. We note your response to our prior comment 10. Please revise the tables on pages 58-9 to include the primary source of research funding for each of 2012 and 2011.

Stock -Based Compensation, page 69

2. Regarding your response to our prior comment 12, we have the following additional comments regarding your disclosure and accounting for stock -based compensation:  As a continuing reminder, since you have not disclosed an estimated offering price we are deferring a final evaluation of stock compensation and other costs

Ramesh Kumar , Ph.D. Onconova Therapeutics, Inc. June 28 , 2013 Page 2

recognized until the estimated offering price is specified. We may have further comments in this regard when the amendment containing that information is filed.  We acknowledge the disclosure in your response letter regarding the 13 “selected comparable companies” considered in estimating your assumed annual volatility rates. Please explain to us why you deemed Enzon Pharmaceuticals to be comparable to you since you state they had five marketed products generating $116 million in annual revenue. In your response, please tell us what your estimated annual volatility rate woul d be if you deleted this company from your sample.  Regarding your fair value common stock valuation at March 31, 2013, please tell us the fair value of common stock at this date inherent in your IPO scenario assuming the IPO is 100% certain and excluding any discounts for weighting other scenarios and lack of marketability.  Please provide in your filing containing the IPO price range, a discussion of each significant factor contributing to the difference between the fair value as of the date of each gran t and the estimated IPO price range. Please reconcile and explain the differences between the mid -point of your estimated offering price range and the fair values included in your analysis.

Recilisib – Acute Radiation Syndromes Treatment, page 99

3. We not e your response to our prior comment 17 and your disclosure that you plan to “continue to seek support from government agencies and to develop recilisib under the FDA Animal Efficacy Rule.” Please expand your disclosure in this section to clarify that all agreements relating to the government funding of recilisib have expired and that no such funding or other obligations remain outstanding.

Notes to Consolidated Financial Statements 15. License and Collaboration Agreements Baxter Agreement, page F -34

4. We acknowledge your response to our prior comment 25. Please revise your disclosure to elaborate on why the license deliverable has standalone value from the research and development services deliverable consistent with your response.

We urge all persons who are responsible for the accuracy and adequacy of the disclosure in the filing to be certain that the filing includes the information the Securities Act of 1933 and all applicable Securities Act rules require. Since the company and its managemen t are in possession of all facts relating to a company’s disclosure, they are responsible for the accuracy and adequacy of the disclosures they have made.

Ramesh Kumar , Ph.D. Onconova Therapeutics, Inc. June 28 , 2013 Page 3

You may contact Jim Peklenk at (202) 551 -3661 or Mark Brunhofer at ( 202) 551 -3638 if you have questi ons regarding comments on the financial statements and related matters. Please contact Austin Stephenson at (202) 551 -3192, Dan Greenspan at (202) 551 -3623 , or me at (202) 551-3715 with any other questions.

Sincerely,
/s/ Jeffrey P. Riedler

Show Raw Text
June 28 , 2013

Via E -mail
Ramesh Kumar, Ph.D.
President and Chief Executive Officer
Onconova Therapeutics, Inc.
375 Pheasant Run
Newtown, PA 18940

Re: Onconova Therapeutics, Inc.
Registration Statement on Form S -1
Filed June 14 , 2013
File No. 333 -189358

Dear Dr. Kumar:

We have r eviewed your registration statement filed June 14, 2013 and your response to
our comments to your confidential draft registration statement submitted on May 3, 2013 and
have the following comments. In some of our comments, we may ask you to provide us with
infor mation so we may better understand your disclosure.

Please respond to this letter by providing the requested infor mation and  amending
your registr ation statement .  If you do  not believe our comments apply to your facts and
circu mstances or do not believe an  amendment is a ppropriate, please tell us why in your
response.

After revie wing the infor mation you provide  in response to these com ments, we may
have additio nal co mments.

Management’s Discussion and Analysis, page 55
Financial Overview, page 58

1. We note your response to our prior comment 10.  Please revise the tables on pages
58-9 to include the primary source of research funding for each of 2012 and 2011.

Stock -Based Compensation, page 69

2. Regarding your response to our prior comment 12, we have the following additional
comments regarding your disclosure and accounting for stock -based compensation:
 As a continuing reminder, since you have not disclosed an estimated offering
price we are deferring a final evaluation of stock compensation and other costs

Ramesh Kumar , Ph.D.
Onconova Therapeutics, Inc.
June 28 , 2013
Page 2

 recognized until the estimated offering price is specified.  We may have
further comments in this regard when the amendment containing that
information is filed.
 We acknowledge the disclosure in your response letter regarding the 13
“selected comparable companies” considered in estimating your assumed
annual volatility rates.   Please explain to us why you deemed Enzon
Pharmaceuticals to be comparable to you since you state they had five
marketed products generating $116 million in annual revenue.  In your
response, please tell us what your estimated annual volatility rate woul d be if
you deleted this company from your sample.
 Regarding your fair value common stock valuation at March 31, 2013, please
tell us the fair value of common stock at this date inherent in your IPO
scenario assuming the IPO is 100% certain and excluding any discounts for
weighting other scenarios and lack of marketability.
 Please provide in your filing containing the IPO price range, a discussion of
each significant factor contributing to the difference between the fair value as
of the date of each gran t and the estimated IPO price range.  Please reconcile
and explain the differences between the mid -point of your estimated offering
price range and the fair values included in your analysis.

Recilisib – Acute Radiation Syndromes Treatment, page 99

3. We not e your response to our prior comment 17 and your disclosure that you plan to
“continue to seek support from government agencies and to develop recilisib under
the FDA Animal Efficacy Rule.”  Please expand your disclosure in this section to
clarify that all  agreements relating to the government funding of recilisib have expired
and that no such funding or other obligations remain outstanding.

Notes to Consolidated Financial Statements
15. License and Collaboration Agreements
Baxter Agreement, page F -34

4. We acknowledge your response to our prior comment 25.  Please revise your
disclosure to elaborate on why the license deliverable has standalone value from the
research and development services deliverable consistent with your response.

We urge all persons who are responsible for the accuracy and adequacy of the disclosure
in the filing to be certain that the filing includes the information the Securities Act of 1933 and
all applicable Securities Act rules require. Since the company and its managemen t are in
possession of all facts relating to a company’s disclosure, they are responsible for the accuracy
and adequacy of the disclosures they have made.

Ramesh Kumar , Ph.D.
Onconova Therapeutics, Inc.
June 28 , 2013
Page 3

 You may contact Jim Peklenk at (202) 551 -3661  or Mark Brunhofer at ( 202) 551 -3638 if
you have questi ons regarding comments on the financial statements and related matters. Please
contact Austin Stephenson at (202) 551 -3192, Dan Greenspan at (202) 551 -3623 , or me at (202)
551-3715 with any other questions.

Sincerely,

         /s/ Jeffrey P. Riedler

Jeffrey P. R iedler
Assista nt Direct or

cc: Via E -mail
David S. Rosenthal, Esq.
Dechert LLP