Bavarian Nordic A/S - Interim Report for the period 1 January to 31 March 2010


·       FDA acceptance of manufacturing facilities leads to the imminent
initiation of IMVAMUNE® smallpox vaccine deliveries to the US Strategic National
Stockpile
·       PROSTVAC(TM) Phase III design outlined upon positive feedback from US
and European regulatory agencies
·       Successful rights issue with net proceeds of approximately DKK 300
million completed

In the first quarter of 2010 Bavarian Nordic generated revenue of DKK 14 million
and recorded a loss before tax of DKK 116 million. The expectations for the
financial result for the full year 2010 are maintained at revenues in the level
of DKK 475 million, and a pre-tax loss in the level of DKK 250 million. As of
31 March 2010 the Group's cash preparedness was DKK 363 million.

Highlights from the period

· IMVAMUNE® deliveries to begin soon upon the recent acceptance from the FDA
     In March 2010, Bavarian Nordic received notification that the U.S. Food and
Drug Administration (FDA) had accepted all the actions taken by the company to
address the observations made during their previous inspection of the
manufacturing facilities. Consequently, delivery of the 20 million doses of
IMVAMUNE® smallpox vaccines to the U.S. Strategic National Stockpile is expected
to commence during first half of 2010.

·       Bavarian Nordic successfully completes end of Phase II meeting for
PROSTVAC(TM)
     In March 2010, the company announced the successful completion of an end of
Phase II meeting with the FDA for the PROSTVAC(TM) programme. The European
Medicines Agency mirrored the input in their Scientific Advice, hence Bavarian
Nordic will proceed to assemble a clinical trial protocol and submit it to the
Special Protocol Assessment (SPA) process with the FDA.

·       PROSTVAC(TM) paper published by the peer-reviewed Journal of Clinical
Oncology
     In January 2010, a paper on the previously reported Phase II study with
PROSTVAC(TM) was published in the prestigious Journal of Clinical Oncology, the
official journal of ASCO.

·       Approximately DKK 300 million raised in successful rights issue
     In February 2010, Bavarian Nordic successfully completed an offering,
generating net proceeds of approximately DKK 300 million. The rights issue
attracted positive attention from both domestic and international investors.

Important events after the period

· US authorities quantifies the requirement for a safer smallpox vaccine
In a recent Broad Agency Announcement, BARDA - the US agency responsible for the
procurement of medical countermeasures, noted the requirement for sufficient
quantity of attenuated smallpox vaccine (e.g. IMVAMUNE®) to protect 66 million
people comprising those for whom traditional smallpox vaccines are
contraindicated.

Anders Hedegaard, President & CEO commented on the interim report: "During first
quarter of 2010 Bavarian Nordic has made substantial progress through the
completion of a number of significant milestones. This has added significant
value to the company and not least to our shareholders, who demonstrated their
robust support to Bavarian Nordic in the successful rights issue at the
beginning of the year. Since then, we have had a strong news flow headed by the
fulfilment of FDA requirements for our manufacturing facilities, leading to the
imminent initiation of delivery of IMVAMUNE® to the US, and by the endorsement
of our planned Phase III programme for PROSTVAC(TM) from the FDA and the
European Medicines Agency."

Conference call
The company will host a conference call tomorrow, Wednesday, April 28 at 2. p.
m. CET. President and CEO, Anders Hedegaard will present the interim results
followed by a Q&A session. Also attending are CFO, Ole Larsen, and Vice
President Investor Relations & Communications, Rolf Sass Sørensen. Dial-in
numbers for the conference call are: Denmark: +45 3271 4607, UK: +44 (0)20
7162 0077. The accompanying presentation is available on the company's website:
www.bavarian-nordic.com <http://www.bavarian-nordic.com/>.

Contact
Anders Hedegaard, President & CEO. Phone +45 23 20 30 64

Management's review

Pipeline

+-------------------+--------------------------+-----------+-------------------+
|PIPELINE           |Programme                 |Status     |Next milestone     |
+-------------------+--------------------------+-----------+-------------------+
|                   |PROSTVAC(TM)              |Phase II   |Phase III (2010)   |
|                   +--------------------------+-----------+-------------------+
|                   |Breast Cancer             |Phase I/II |Initiate new Phase |
|Cancer             |(MVA-BN(®)-HER2)          |           |I/II study (2010)  |
|                   +--------------------------+-----------+-------------------+
|                   |Prostate Cancer (MVA-BN(®)|Phase I/II |Phase I/II data    |
|                   |PRO)                      |           |update (2010)      |
+-------------------+--------------------------+-----------+-------------------+
|                   |Smallpox (IMVAMUNE(®))    |Phase II   |Initiate Phase III |
|Biodefence         |                          |           |(2010)             |
|                   +--------------------------+-----------+-------------------+
|                   |Anthrax                   |Preclinical|Phase I (2010)     |
+-------------------+--------------------------+-----------+-------------------+
|                   |HIV multiantigen          |Phase I/II |Identify partner   |
|                   |                          |           |for full Phase II  |
|Infectious diseases+--------------------------+-----------+-------------------+
|                   |Measles and RSV           |Phase I    |Phase I data (H2,  |
|                   |                          |           |2010)              |
+-------------------+--------------------------+-----------+-------------------+


Biodefence

IMVAMUNE® - smallpox vaccine

Bavarian Nordic fulfils FDA requirements to support the delivery of IMVAMUNE® to
the US Government
In March 2010, Bavarian Nordic received notification that the U.S. Food and Drug
Administration (FDA) had accepted all the actions taken by the company to
address the observations made during the inspection of the manufacturing
facilities in 2009. This was the last step along with the clinical and
preclinical data that will be used to potentially support the use of IMVAMUNE®
following a declared emergency. Subsequently, the company has begun to scale-up
production, so the 20 million doses will be produced and delivered according to
the contract. The first deliveries are expected to take place during first half
of 2010 as previously communicated.

US quantifies the requirement for a safer smallpox vaccine
In a recent Broad Agency Announcement, BARDA - the US authority responsible for
the procurement of medical countermeasures, noted the requirement for sufficient
quantity of attenuated smallpox vaccine (e.g. IMVAMUNE®) to protect 66 million
people comprising those for whom smallpox vaccine is contraindicated.

Cancer

PROSTVAC(TM) - therapeutic prostate cancer vaccine

Bavarian Nordic successfully completes end of Phase II meeting for PROSTVAC(TM)
In March 2010, the company concluded upon the Scientific Advice from the
European Medicines Agency and the end of Phase II meeting with the FDA for the
PROSTVAC(TM) programme. Both agencies expressed general agreement with the
proposed Phase III clinical programme of PROSTVAC(TM). Based on the consolidated
feedback Bavarian Nordic will proceed to assemble a clinical trial protocol and
submit it to the Special Protocol Assessment (SPA) process with the FDA. The
final clinical protocol will be based on the outcome of this process.

Based on the consolidated feedback, Bavarian Nordic is planning to achieve
marketing approval for PROSTVAC(TM) via a single global, strongly powered
clinical trial that is expected to enrol about 1,200 patients. The study will be
placebo-controlled and enrol patients with asymptomatic or minimally
symptomatic, metastatic castration-resistant prostate cancer (mCRPC), similar to
the patient population studied in the company's placebo-controlled Phase II
study.

PROSTVAC(TM) paper published by the peer-reviewed Journal of Clinical Oncology
In January 2010, a paper on the previously reported Phase II study with
PROSTVAC(TM) was published in the prestigious Journal of Clinical Oncology, the
official journal of ASCO.

Other issues

Successful rights issue generates net proceeds of approximately DKK 300 million
In February 2010, Bavarian Nordic completed an offering in which 3,960,307 new
shares were subscribed, corresponding to a subscription rate of 99.6%.

The new shares were subscribed at DKK 80 per share, resulting in gross proceeds
to Bavarian Nordic of DKK 317 million, equivalent to net proceeds of DKK 302
million after deduction of expenses related to the offering.

Following registration of the new shares, Bavarian Nordic's nominal share
capital will be DKK 119,120,520 corresponding to 11,912,052 shares with a
nominal value of DKK 10 each.

Bavarian Nordic and Oxford BioMedica settle all legal disputes on MVA-BN®
In January 2010 Bavarian Nordic and Oxford BioMedica reached a global settlement
ending the legal disputes between the parties on matters relating to MVA-BN®.

Under the agreement, Bavarian Nordic granted a license to its MVA-BN® patents in
return for Oxford BioMedica making milestone payments and royalties.

Under the settlement, the terms of which are confidential, all pending
litigation will cease and all oppositions filed at the European Patent Office by
Oxford BioMedica will be withdrawn.
Financial statement for the period (1 January - 31 March 2010, un-audited)
The comparison figures for the same period 2009 are stated in parenthesis.

The revenue totalled DKK 14 million (DKK 17 million) in the first quarter. The
revenue derives mainly from the sale under the RFP-2 contract, DKK 12 million,
and the RFP contract for freeze-dried IMVAMUNE®, DKK 2 million.

Production costs totalled DKK 63 million (DKK 41 million) in the first quarter.

The Group's research and development costs totalled DKK 40 million (DKK 36
million) in the first quarter excluding development costs from the RFP-2 and
RFP-3 contracts and the RFP contract for freeze-dried IMVAMUNE® of DKK 10
million, of which DKK 5 million are capitalized as intangible assets under
construction.

Distribution costs totalled DKK 6 million (DKK 6 million) and administrative
costs totalled DKK 21 million (DKK 23 million).

Income before tax is a deficit of DKK 116 million (deficit of DKK 83 million).

Net result in the first quarter is a deficit of DKK 93 million (deficit DKK 66
million).

The IMVAMUNE® inventory totalled DKK 216 million (DKK 79 million).

As of 31 March 2010 the Group's cash preparedness was DKK 363 million (DKK 647
million). Cash flow from operations is negative with DKK 124 million (DKK -132
million). Cash flow from investment activities is negative with DKK 44 million
(DKK 33 million) and cash flow from financing activities is DKK 290 million (DKK
-4 million). The net change in cash and cash equivalents is DKK 122 million (DKK
-103 million).

The Group's equity as of 31 March 2010 was DKK 900 million (DKK 903 million).
The right issue in first quarter 2010 increased the equity by DKK 302 million
net after related cost.

Financial expectations
Bavarian Nordic maintains its expectations for the financial result for 2010.
Management expects revenue at the level of DKK 475 million, and a pre-tax loss
at the level of DKK 250 million. Revenue will primarily be generated from the
delivery of IMVAMUNE® to the United States under the RFP-3 contract and billing
of the continuation of the RFP-2 contract and the RFP contract for freeze-dried
IMVAMUNE®.

The cash preparedness at year-end is expected to be in the range of DKK 225
million to DKK 275 million. This is based upon the assumption that a credit
facility in the amount of DKK 150 million to DKK 200 million to finance working
capital is obtained.

Statement from the Board of Directors and Corporate Management
The Board of Directors and Corporate Management have, today reviewed and
approved Bavarian Nordic A/S' interim report for the period 1 January to 31
March 2010.

The interim report has been prepared in accordance with IAS 34 "Presentation of
interim reports" as adopted by the EU and additional Danish disclosure
requirements for interim reports of listed companies, including those of NASDAQ
OMX Copenhagen. The interim report has not been audited or reviewed by the
Company's auditors.

In our opinion, the interim report gives a true and fair view of the group's
assets and liabilities and financial position as of 31 March 2010 and the
results of the group's activities and cash flows for the period 1 January to 31
March 2010.

In our opinion, the management's review provides a true and fair description of
the development in the group's activities and financial affair, the results for
the period and the group's financial position as a whole as well as a
description of the most important risks and uncertainty factors faced by the
group.


Kvistgård, 27 April 2010



Corporate Management:



Anders Hedegaard
President and CEO



Board of Directors:



Asger Aamund
Chaiman of the Board


Claus Bræstrup
Erling Johansen
Gerard van Odijk
Flemming Pedersen

Forward-looking statements
This announcement includes "forward-looking statements" that involve risks,
uncertainties and other factors, many of which are outside of our control that
could cause actual results to differ materially from the results discussed in
the forward-looking statements. Forward-looking statements include statements
concerning our plans, objectives, goals, future events, performance and/or other
information that is not historical information. We undertake no obligation to
publicly update or revise forward-looking statements to reflect subsequent
events or circumstances after the date made, except as required by law.

About Bavarian Nordic
Bavarian Nordic A/S is a leading industrial biotechnology company developing and
producing novel vaccines for the treatment and prevention of life-threatening
diseases with a large unmet medical need. The company's pipeline is focused in
the three areas; biodefence, cancer and infectious diseases, and includes seven
development programmes. Two programmes are under preparation for Phase III:
IMVAMUNE®, a third-generation smallpox vaccine is being developed under a
contract with the US government, and PROSTVAC(TM), a therapeutic vaccine for
advanced prostate cancer is being developed under a collaboration agreement with
the National Cancer Institute.

Bavarian Nordic is listed on NASDAQ OMX Copenhagen under the symbol BAVA.

For more information please visit www.bavarian-nordic.com
<http://www.bavarian-nordic.com/>



[HUG#1408766]


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