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SEC Company Response from KOSAN BIOSCIENCES INC (CIK 0001110206) — Oct 25, 2005

KOSAN BIOSCIENCES INC (CIK 0001110206)
Date: Oct. 25, 2005 · CIK: 0001110206 · Accession: 0001193125-05-207778

AI Filing Summary & Sentiment

File numbers found in text: 000-31633

Referenced dates: August 24, 2005

Date
October 24, 2005
Author
Not clearly detected
Form
CORRESP
Company
KOSAN BIOSCIENCES INC (CIK 0001110206)

Letter

Division of Corporation Finance Re: Kosan Biosciences Incorporated Form 10-K for Fiscal Year Ended December 31, 2004 (the “Form 10-K”) Filed March 16, 2005 File Number 000-31633

Dear Ms. Parikh:

On behalf of our client, Kosan Biosciences Incorporated (the “Company” or “Kosan”), in response to our discussions on October 4, 2005, October 11, 2005 and October 20, 2005 related to a comment received from the staff of the Commission (the “Staff”) by letter dated August 24, 2005 with respect to the Form 10-K, following is a revised table summarizing the current status and the costs incurred during (i) each period presented and (ii) from inception to date, in each case for the Company’s major research and development projects.

Related R&D expenses

Years ended December 31,

Related R&D expenses for the nine months ended September 30,

Inception - September 30, 2005

Development program

Clinical development:

Epothilones

$ 12,101

$ 14,038

$ 8,848

$ 7,840

$ 9,500

$ 46,212

Hsp90 inhibitors

5,432

—

—

7,054

3,269

12,486

Total clinical development

17,533

14,038

8,848

14,894

12,769

58,698

Research and preclinical:

Epothilones

4,655

5,032

2,112

4,520

24,770

Hsp90 inhibitors

—

3,828

3,183

—

7,940

Other(1)

17,987

13,891

14,235

12,891

13,342

101,529

Total research and preclinical

22,642

22,751

19,530

13,567

17,862

134,239

Total research and development

$ 40,175

$ 36,789

$ 28,378

$ 28,461

$ 30,631

$ 192,937

(1) Other” constitutes internal research and development costs for our early stage product candidates in the areas of gastrointestinal motility, infectious disease, cancer and technology development. For the years ended December 31, 2004, 2003 and 2002, “Other” expenses consisted primarily of allocated personnel-related expenses of approximately $8.1 million, $5.7 million and $6.8 million, allocated facility-related expenses of approximately $5.4 million, $3.8 million and $3.5 million and allocated lab consumables of approximately $1.4 million, $1.0 million and $905,000, respectively. During the nine months ended September 30, 2005 and 2004, “Other” expenses consisted primarily of allocated personnel-related expenses of approximately $6.1 million and $5.9 million, allocated facility-related expenses of approximately $4.1 million and $4.0 million and allocated lab consumables of $865,000 and $1.0 million, respectively. During the period from inception through September 30, 2005, “Other” expenses consisted primarily of allocated personnel-related expenses of approximately $51.5 million, allocated facility-related expenses of approximately $25.1 million and allocated lab consumables of $7.5 million.

October 24, 2005

Page Two

We would appreciate confirmation that inclusion of this table and the following new disclosure in the Company’s Quarterly Report on Form 10-Q for quarter ended September 30, 2005, and as appropriately updated in future Quarterly Reports on Form 10-Q and Annual Reports on Form 10-K, will address the comment received from the Staff and related discussions.

New Disclosure:

The Company is unable to estimate the nature, timing or costs to complete its major research and development projects, or when material net cash inflows to the Company could be expected to commence, if ever, due to the numerous risks and uncertainties associated with developing pharmaceutical products. These risks and uncertainties include those discussed in this report under the heading “Risk Factors That May Affect Results of Operations and Financial Condition”.

The Company would also continue to include a summary the current development phase of each of the Company’s most advanced product candidates, when the current phase was initiated and the typical duration of each phase of development, substantially as currently presented in the Company’s Form 10-K.

***

Please advise us if we can provide any further information or assistance to facilitate your review. Please continue to direct any further comments or questions regarding this matter to me at (650) 843-5180.

Sincerely,
Cooley Godward LLP

Show Raw Text
CORRESP
1
filename1.htm

Correspondence Letter

ATTORNEYS AT LAW

 Broomfield, CO

 720
566-4000

 Reston, VA

 703 456-8000

 San Diego, CA

 858 550-6000

 San Francisco, CA

 415 693-2000

 Five Palo Alto Square

 3000 El Camino
Real

 Palo Alto, CA

 94306-2155

 Main      650 843-5000

 Fax         650 849-7400

October 24, 2005

www.cooley.com

 VIA FACSIMILE AND EDGAR

 Sasha Parikh

 Division of Corporation Finance

 U.S. Securities and Exchange Commission

 450 Fifth Street, N.W.

 Washington, D.C. 20549

Re:
Kosan Biosciences Incorporated

 Form 10-K for
Fiscal Year Ended December 31, 2004 (the “Form 10-K”)

 Filed March 16, 2005

 File Number 000-31633

 Dear Ms. Parikh:

 On behalf of our client, Kosan Biosciences Incorporated (the “Company” or “Kosan”), in response to our discussions on October 4,
2005, October 11, 2005 and October 20, 2005 related to a comment received from the staff of the Commission (the “Staff”) by letter dated August 24, 2005 with respect to the Form 10-K, following is a revised table
summarizing the current status and the costs incurred during (i) each period presented and (ii) from inception to date, in each case for the Company’s major research and development projects.

 Related R&D expenses

 Years ended December 31,

Related R&D expenses for the
nine months ended September 30,

Inception -
September 30, 2005

 Development program

2004

2003

2002

2005

2004

 Clinical development:

 Epothilones

$
12,101

$
14,038

$
8,848

$
7,840

$
9,500

$
46,212

 Hsp90 inhibitors

5,432

—

—

7,054

3,269

12,486

 Total clinical development

17,533

14,038

8,848

14,894

12,769

58,698

 Research and preclinical:

 Epothilones

4,655

5,032

2,112

310

4,520

24,770

 Hsp90 inhibitors

—

3,828

3,183

366

—

7,940

 Other(1)

17,987

13,891

14,235

12,891

13,342

101,529

 Total research and preclinical

22,642

22,751

19,530

13,567

17,862

134,239

 Total research and development

$
40,175

$
36,789

$
28,378

$
28,461

$
30,631

$
192,937

(1)
Other” constitutes internal research and development costs for our early stage product candidates in the areas of gastrointestinal motility, infectious disease, cancer and
technology development. For the years ended December 31, 2004, 2003 and 2002, “Other” expenses consisted primarily of allocated personnel-related expenses of approximately $8.1 million, $5.7 million and $6.8 million, allocated
facility-related expenses of approximately $5.4 million, $3.8 million and $3.5 million and allocated lab consumables of approximately $1.4 million, $1.0 million and $905,000, respectively. During the nine months ended September 30, 2005 and
2004, “Other” expenses consisted primarily of allocated personnel-related expenses of approximately $6.1 million and $5.9 million, allocated facility-related expenses of approximately $4.1 million and $4.0 million and allocated lab
consumables of $865,000 and $1.0 million, respectively. During the period from inception through September 30, 2005, “Other” expenses consisted primarily of allocated personnel-related expenses of approximately $51.5 million,
allocated facility-related expenses of approximately $25.1 million and allocated lab consumables of $7.5 million.

 October 24, 2005

 Page Two

 We would appreciate confirmation that inclusion of this table and the following new disclosure in the Company’s Quarterly Report on Form 10-Q for quarter ended
September 30, 2005, and as appropriately updated in future Quarterly Reports on Form 10-Q and Annual Reports on Form 10-K, will address the comment received from the Staff and related discussions.

 New Disclosure:

 The Company is unable to estimate the nature, timing or costs to complete its major research and development projects, or
when material net cash inflows to the Company could be expected to commence, if ever, due to the numerous risks and uncertainties associated with developing pharmaceutical products. These risks and uncertainties include those discussed in this
report under the heading “Risk Factors That May Affect Results of Operations and Financial Condition”.

 The Company would also continue to include a summary the current development phase of each of the Company’s most advanced product candidates, when the current phase
was initiated and the typical duration of each phase of development, substantially as currently presented in the Company’s Form 10-K.

 ***

 Please advise us if we can provide any further information or assistance to facilitate your review. Please continue to direct any further comments or questions regarding this matter to me at (650) 843-5180.

 Sincerely,

Cooley Godward LLP

 /s/ Suzanne Sawochka Hooper

By:

Suzanne Sawochka Hooper, Partner

cc:
Susan M. Kanaya