Pharma sector to grow fastest since 2014; FY19 profit set to jump 20-22%
After
a bruising two year, the domestic pharmaceutical sector is set for a sharp
turnaround in the new fiscal year with a 20-22 per cent growth in operating
profit - the fastest pace since 2014, while revenue may grow at 9-11 per cent,
according to a report. "The projected good run is premised on a decline in
regulatory alerts for larger companies as well as a bigger pipeline of
high-value drugs compared to the past two years. Operating income and profit
will see a course reversal with a 20-22 per cent growth, while revenue may clip
at 9-11 per cent," rating agency Crisil said in a report.
This will be
primarily on the back of strong growth in the overseas market, particularly in
the regulated markets of the US and the EU, while the domestic market will
continue its healthy growth in the past years, it said.
It can be noted
that although exports account for only 50 per cent of revenue for the domestic
pharma industry, its contribution at the operating profit is higher owing to
relatively superior profitability of products sold in regulated markets and
that the hemorrhage over the past two years can be pinned squarely on dwindling
exports to regulated markets, particularly these two markets.
The US and the
EU together account for over 90 per cent of the regulated market exports and
close to 50 per cent of formulation exports for the domestic companies.
However, the
report warns that lower generic opportunity, rising competition, supplier
consolidation, and increase in regulatory alerts on domestic plants are the
major headwinds for the industry.
Noting that
relief from regulatory alerts will result to increase in abbreviated new drug
application (ANDA) flows, the report says rising competition and supplier
consolidation and the resultant pricing pressure, will continue to impact
exports to these key markets in FY19.
Sales to the US
and the EU are expected to rise 7 per cent against a decline of 3 per cent
between fiscals 2016 and 2018. One of the factors working in favour of larger
pharma companies is a marked reduction in the number of regulatory alerts in 2017,
a welcome change from 2015 and 2016.
Official action
indicated (OAI) came down significantly to 16 in 2017 from 28 in 2014 due to
the efforts taken by large formulation companies during these years towards
remediation.
Issuance of an
OAI indicates objectionable conditions were found and will result in regulatory
and/or administrative sanctions by the US. Typically, non-closure of an OAI
results in a warning letter or an import alert. Increased efforts towards
remediation have also resulted in close-out of some regulatory alerts for big
players in the past one year.
"We
expect this to continue this year for larger players, allowing them to receive
new ANDAs which were stalled owing to these alerts, thereby improving
exports," it said.
Domestic
companies are also likely to benefit from their higher R&D investments over
the past few years. Along with developing capabilities through inorganic route,
domestic exporters have been focusing on strengthening their in-house product
pipeline via R&D due to higher pricing pressure on conventional generics
and lower patent expiry opportunity.
They are also
shifting focus from conventional generics to complex generics and biosimilars
as competition within the conventional generics space is intensifying. The move
also ensures healthy growth prospects.
This, though,
requires considerably higher R&D investment. For example, cost of
developing a biosimilar is around USD 150 million compared to USD 1-5 million
to develop a generic drug. While the cost of developing niche complex drugs and
biosimilars is substantially high, the potential opportunity and profitability
are commensurate.
The higher
investment in niche and complex drugs over the past few years is expected to
start bearing fruit in fiscal 2019. The number of high value drugs likely to be
launched in FY19 is three times over FY18.
Signs
of recovery are already visible, with some high value drugs already approved in
the past two-three months. For instance, Biocon received approval in December
2017 from the US to launch its biosimilar version of Herceptin-developed
jointly with Mylan. Sun Pharmaceuticals got a nod in March 2017 to launch its
specialty drug Tildrakizumb.
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